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Human Genetic Disorders That Feature Premature Onset and Accelerated Progression of Biological Aging

  • Chapter
The Genetics of Aging

Abstract

Despite a burgeoning number of recent investigations and increasingly rigorous scrutiny, a universally acceptable definition of normal biological aging is still not available. The origins of senescence remain enigmatic, and little agreement exists regarding its true nature. While most would accept as genuine aging phenomena the diverse processes of hair graying, wrinkling of skin, and arteriosclerosis, they would, on the other hand, reserve embryogenesis, somatic growth, and pubescence for development. Both kinds of phenomena are clearly time-dependent, but the interface between them is often blurred (Goldstein, S., 1971a). The conceptual difficulty is exemplified by the frequent juxtaposition of involution and new development, even at early and middle stages of the life span (Saunders and Fallon, 1966). Cogent examples are the placenta vs. the fetus during gestation and the replacement of deciduous teeth by permanent dentition during infancy. During childhood, atrophy of the thymus occurs when virtually all other organs are growing and maturing, while the menopausal ovary involutes relatively abruptly in comparison with other organs in the middle-aged female. One could invoke examples of involution at the molecular level such as the loss during fetal life of various proteins including ϒ-hemoglobin, carcinoembryonic antigen, α-fetoprotein, and others (Gold, 1971). In short, attempts to delineate the point at which development is succeeded by aging may be futile, since both processes probably operate along the same continuum.

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References

  • Alberti, K. G., Young, J. D., and Hockaday, T. O., 1974, Werner’s syndrome: Metabolic observations, Proc. R. Soc. Med. 67:36–38.

    PubMed  CAS  Google Scholar 

  • Alton, D. J., McDonald, P., and Reilly, B. J., 1972, Cockayne’s syndrome: A report of three cases, Radiology 102:403–406.

    PubMed  CAS  Google Scholar 

  • Ammann, A. J., Cain, W. A., Ishizaka, K., Hong, R., and Good, R. A., 1969, Immunoglobulin E deficiency in ataxia-telangiectasia, N. Engl. J. Med. 281:469–472.

    PubMed  CAS  Google Scholar 

  • Andres, W., Pozefsky, T., Swerdloff, R. S., and Tobin, J. D., 1975, Effect of aging on carbohydrate metabolism, Adv. Metab. Disord. Suppl. 1:349–355.

    Google Scholar 

  • Atkins, L., 1954, Progeria: Report of a case with post-mortem findings, N. Engl. J. Med. 250:1065–1069.

    PubMed  CAS  Google Scholar 

  • Bach, F. H., and van Rood, J. J., 1976, The major histocompatibility complex: Genetics and biology, N. Engl. J. Med. 295: 806–813, 872-878, 927-936.

    PubMed  CAS  Google Scholar 

  • Balci, S., Say, B., and Kinik, E., 1970, Werner’s syndrome, Turk. J. Pediatr. 12:89–97.

    PubMed  CAS  Google Scholar 

  • Benditt, E. P., and Benditt, J. M., 1973, Evidence for a monoclonal origin of human atherosclerotic plaques, Proc. Natl. Acad. Sci. U.S.A. 70:1753–1756.

    PubMed  CAS  Google Scholar 

  • Bhakoo, O. N., Garg, S. K., and Sehgal, V. N., 1965, Progeria with unusual ocular manifestations: Report of a case with a review of the literature, Indian Pediatr. 2:164–169.

    PubMed  CAS  Google Scholar 

  • Bingham, H. G., and Anderson, P. G., 1970, Coverage of cutaneous ulcers in Werner’s syndrome, Acta Derm.-Venereol. 50:237–239.

    PubMed  CAS  Google Scholar 

  • Blinstrub, R. W., Lehman, R., and Steinberg, T. H., 1964, Poikiloderma congenitale: Report of two cases, Arch. Dermatol. 89:659–664.

    PubMed  CAS  Google Scholar 

  • Blizzard, R. M., 1965, Dwarfism, in: Diagnosis and Treatment of Endocrine Disorders in Childhood and Adolescence (L. Wilkins, ed.), pp. 160–194, Charles C. Thomas, Springfield, Illinois.

    Google Scholar 

  • Block, B., and Stauffer, H., 1929, Skin diseases of endocrine system (dyshormonal dermatoses): Poikiloderma-like changes in connection with underdevelopment of the sexual glands and dystrophia adiposogenitalis, Arch. Dermatol. Syphilol. 19:22–34.

    Google Scholar 

  • Boder, E., and Sedgwick, R. P., 1958, Ataxia-telangiectasia: A familial syndrome of progressive cerebellar ataxia, oculocutaneous telangiectasia and frequent pulmonary infection, Pediatrics 21:526–554.

    PubMed  CAS  Google Scholar 

  • Bottomley, W. K., and Box, J. M., 1976, Dental anomalies in the Rothmund-Thomson syndrome: Report of a case, Oral Surg. 4:321–326.

    Google Scholar 

  • Boué, A., Boué, J., Cure, S., Deluchat, C., and Perraudin, N., 1975, In vitro cultivation of cells from aneuploid human embryos: Initiation of cell lines and longevity of the culture, In Vitro 11:409–413.

    PubMed  Google Scholar 

  • Boyd, M. W. J., and Grant, A. P., 1959, Werner’s syndrome (progeria of the adult): Further pathological and biochemical observations, Br. Med. J. 2:920–925.

    PubMed  CAS  Google Scholar 

  • Bradley, M. O., Erickson, L. C., and Kohn, K. W., 1976, Normal DNA strand rejoining and absence of DNA crosslinking in progeroid and aging human cells, Mutat. Res. 37:279–292.

    PubMed  CAS  Google Scholar 

  • Brautbar, C., Pellegrino, M. A., Ferrone, S., Reisfeld, R. A., Payne, R., and Hayflick, L., 1973, Fate of HL-A antigens in aging cultured human diploid cell strains. II. Quantitative absorption studies, Exp. Cell Res. 78:367–375.

    PubMed  CAS  Google Scholar 

  • Bristow, J. H., 1973, Werner’s syndrome: Clinical features and cataract surgery, S. Afr. Med. J. 47:566–569.

    PubMed  CAS  Google Scholar 

  • Brodrick, J. D., and Dark, A. J., 1973, Corneal dystrophy in Cockayne’s syndrome, Br. J. Opthalmol. 57:391–399.

    CAS  Google Scholar 

  • Bullock, J. D., and Howard, R.O., 1973, Werner’s syndrome, Arch. Ophthalmol. 90:53–56.

    PubMed  CAS  Google Scholar 

  • Burch, P. R. J., and Milunsky, A., 1969, Early-onset diabetes mellitus in general and Down’s syndrome populations: Genetics, etiology, and pathogenesis, Lancet 1:554–558.

    PubMed  CAS  Google Scholar 

  • Burnet, F. M., 1974, Intrinsic Mutagenesis: A Genetic Approach to Aging, John Wiley & Sons, New York.

    Google Scholar 

  • Burnett, J. W., 1968, Werner’s syndrome, South. Med. J. 61:207–209.

    PubMed  CAS  Google Scholar 

  • Cahill, G. F., 1975, Disorders of carbohydrate metabolism, in: Textbook of Medicine (P. B. Beeson and W. McDermott, eds.), pp. 1599-1619, W. B. Saunders Co., Philadelphia. Cahill, G. F., Etzwiler, D. D., and Freinkel, N., 1976, “Control” and diabetes, N. Engl. J. Med. 294:1004–1005.

    Google Scholar 

  • Carr, D. H., 1975, Cytogenetics and the pathologist, Pathobiol. Annu. 10:93–144.

    CAS  Google Scholar 

  • Chaganti, R. S. K., Schonberg, S., and German, J., 1974, A manyfold increase in sister chromatid exchanges in Bloom’s syndrome lymphocytes, Proc. Natl. Acad. Sci. U.S.A. 71:4508–4512.

    PubMed  CAS  Google Scholar 

  • Childs, B., and Der Kaloustian, V. M., 1968, Genetic heterogeneity, N. Engl. J. Med. 279: 1205–1212, 1267-1279.

    PubMed  CAS  Google Scholar 

  • Cleaver, J. E., 1970, DNA damage and repair in light-sensitive human skin disease, J. Invest. Dermatol. 54:181–195.

    PubMed  CAS  Google Scholar 

  • Cleaver, J. E., and Bootsma, D., 1975, Xeroderma pigmentosum: Biochemical and genetic characteristics, Annu. Rev. Genet. 9:19–38.

    PubMed  CAS  Google Scholar 

  • Cleaver, J. E., Bootsma, D., and Friedberg, E., 1975, Human diseases with genetically altered DNA repair processes, Genetics 79:215–225.

    PubMed  Google Scholar 

  • Cockayne, E. A., 1936, Dwarfism with retinal atrophy and deafness, Arch. Dis. Child. 11:1–8.

    PubMed  CAS  Google Scholar 

  • Cohen, M. M., Shaham, M., Dagan, J., Shmueli, E., and Kohn, G., 1975, Cytogenetic investigations in families with ataxia-telangiectasia, Cytogenet. Cell Genet. 15:338–356.

    PubMed  CAS  Google Scholar 

  • Cole, H. N., Giffen, H. K., Simmons, J. T., and Stroud, G. M., III, 1945, Congenital cataracts in sisters with congential ectoderma dysplasia, J. Am. Med. Assoc. 129:723–728.

    Google Scholar 

  • Coles, W. H., 1969, Ocular manifestations of Cockayne’s syndrome, Am. J. Ophthalmol. 67:762–764.

    PubMed  CAS  Google Scholar 

  • Comfort, A., 1964, Ageing: The Biology of Senescence, Holt, Rinehart & Winston, New York.

    Google Scholar 

  • Comfort, A., 1969, Test-battery to measure ageing-rate in man, Lancet 2:1411–1415.

    PubMed  CAS  Google Scholar 

  • Cotton, R. B., Keats, T. E., and McCoy, E. E., 1970, Abnormal blood glucose regulation in Cockayne’s syndrome, Pediatrics 46:54–60.

    PubMed  CAS  Google Scholar 

  • Cox, R. P., 1974, Cell Communication, John Wiley & Sons, New York.

    Google Scholar 

  • Crapper, D. R., Dalton, A. J., Skopitz, M., Scott, J. W., and Hachinski, V. C., 1975, Alzheimer degeneration in Down syndrome: Electrophysiologic alterations and histopathologic findings, Arch. Neurol. 33:618–623.

    Google Scholar 

  • Creutzfeldt, W., Kobberling, J., and Neel, J. V. (eds.), 1975, The Genetics of Diabetes Mellitus, Springer-Verlag, New York.

    Google Scholar 

  • Cristofalo, V. J., 1972, Animal cell cultures as a model system for the study of aging, Adv. Gerontol. Res. 4:45–79.

    CAS  Google Scholar 

  • Crome, L., and Kanjilal, G. C., 1971, Cockayne’s syndrome: Case report, J. Neurol. Neurosurg. Psychiatry 34:171–178.

    PubMed  CAS  Google Scholar 

  • Cunliffe, P. N., Mann, J. R., Cameron, A. H., Roberts, K. D., and Ward, H. W. C., 1975, Radio sensitivity in ataxia telangiectasia, Br. J. Radiol. 48:374–376.

    Google Scholar 

  • Dalton, A. J., Crapper, D. R., and Schlotterer, G. R., 1974, Alzheimer’s disease in Down’s syndrome: Visual retention deficits, Cortex 10:366–377.

    PubMed  CAS  Google Scholar 

  • Danes, B. S., 1971, Progeria: A cell culture study on aging, J. Clin. Invest. 50:2000–2003.

    PubMed  CAS  Google Scholar 

  • DeBusk, F. L., 1972, The Hutchinson-Gilford progeria syndrome: Report of four cases and review of the literature, J. Pediatr. 80(Part 2):695–724.

    Google Scholar 

  • Degreef, H., 1971, The Werner syndrome, Dermatologica 142:45–49.

    PubMed  CAS  Google Scholar 

  • Diem, E., 1975, The Rothmund-Thomson syndrome: A case report, Hautarzt 26:425–429.

    PubMed  CAS  Google Scholar 

  • Down, J. L. H., 1866, Observations on ethnic classification of idiots, Clin. Lect. Rep. London Hosp. 3:259–262.

    Google Scholar 

  • Driban, N. E., and Bertranou, E. G., 1975, Adult progeria (Werner’s syndrome), Med. Cutanea 3:213–222.

    CAS  Google Scholar 

  • Elmore, E., and Swift, M., 1976a, Growth of cultured cells from patients with Fanconi’s anemia, J. Cell. Physiol. 87: 229–234.

    Google Scholar 

  • Elmore, E., and Swift, M., 1976b, Growth of cultured cells from patients with ataxiatelangiectasia, J. Cell. Physiol. 89: 429–432.

    PubMed  CAS  Google Scholar 

  • Engle, E., and Forbes, A. P. 1965, Cytogenetic and clinical findings in 48 patients with congenitally defective or absent ovaries, Medicine (Baltimore) 44:135–164.

    Google Scholar 

  • Epstein, C. J., Martin, G. M., Schultz, A. L., and Motulsky, A. G., 1966, Werner’s syndrome: A review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process, Medicine (Baltimore) 45:177–221.

    CAS  Google Scholar 

  • Epstein, J., Williams, J. R., and Little, J. B., 1973, Deficient DNA repair in human progeroid cells, Proc. Natl. Acad. Sci. U.S.A. 70:977–981.

    PubMed  CAS  Google Scholar 

  • Epstein, J., Williams, J. R., and Little, J. B., 1974, Rate of DNA repair in progeric and normal human fibroblasts, Biochem. Biophys. Res. Commun. 59:850–856.

    PubMed  CAS  Google Scholar 

  • Fajans, S. S., Floyd, J. C., Tattersall, R. B., Williamson, J. R., Pek, S., and Taylor C. I., 1976, The various faces of diabetes in the young, Arch. Intern. Med. 136:194–202.

    PubMed  CAS  Google Scholar 

  • Faye, I., Ruscher, H., Marchand, J. P., Bloc, G., and Toure, M. F., 1973, A case of Werner’s syndrome, Bull. Soc. Med. Afr. Noire Lang. Fr. 18:564–566.

    PubMed  CAS  Google Scholar 

  • Feigin, R. D., Vietti, T. J., Wyatt, R. G., Kaufman, D. G., and Smith, C. H., 1970, Ataxia telangiectasia with granulocytopenia, J. Pediatr. 77:431–438.

    PubMed  CAS  Google Scholar 

  • Feingold, M., and Kidd, R., 1971, Progeria and scleroderma in infancy, Am. J. Dis. Child. 122:61–62.

    PubMed  CAS  Google Scholar 

  • Felig, P., Wahren, J., Sherwin, R., and Hendler, R., 1976, Insulin, glucagon, and somatostatin in normal physiology and diabetes mellitus, Diabetes 25:1091–1099.

    PubMed  CAS  Google Scholar 

  • Ferrari-Sacco, A., Carolei, P., Emanuele, B., Marasso, A., and Marengo, G., 1972, Etiopathogenetic, clinical and anatomo-histological notes on a very rare form of congenital anomaly (Werner’s syndrome or Rothmund-Thomson syndrome) associated with pulmonary tuberculosis, Minerva Med. 63:2563–2573.

    PubMed  CAS  Google Scholar 

  • Finkelberg, R., 1976, Studies on cells from patients with Fanconi’s anemia, Ph.D. thesis, University of Toronto.

    Google Scholar 

  • Fleischmajer, R., and Nedwich, A., 1973a, Progeria (Hutchinson-Gilford), Arch. Dermatol. 107: 253–258.

    PubMed  CAS  Google Scholar 

  • Fleischmajer, R., and Nedwich, A., 1973b, Werner’s syndrome, Am. J. Med. 54: 111–118.

    PubMed  CAS  Google Scholar 

  • Forbes, A. P., and Engel, E., 1963, The high incidence of diabetes mellitus in 41 patients with onadal dysgenesis and their close relatives, Metabolism 12:428–439.

    PubMed  CAS  Google Scholar 

  • Ford, C. E., Kones, K. W., Polani, P. E., DeAlmeida, J. C., and Briggs, J. H., 1959, A sex chromosome anomaly in a case of gonadal dysgenesis (Turner’s syndrome) Lancet 1:711.

    PubMed  CAS  Google Scholar 

  • Franceschetti, A., 1953, Les dysplasies ectodermiques et les syndromes héréditaires apparantes, Dermatologica 106:129–156.

    PubMed  CAS  Google Scholar 

  • Franks, L. M., 1972, The ultrastructure of tissue culture cells, Symp. Biol. Hung. 14:31–35.

    Google Scholar 

  • Fraser, G. R., and Friedmann, A. I., 1967, The Causes of Blindness in Childhood: A Study of 776 Children with Severe Visual Handicaps, Johns Hopkins University Press, Baltimore.

    Google Scholar 

  • Fratontoni, J. C., Hall, C. W., and Neufeld, E. F., 1968, Hurler and Hunter syndromes: Mutual correction of the defect in cultured fibroblasts, Science 162:570–572.

    Google Scholar 

  • Frenkel, G., 1970, Mucosal atrophy with special reference to the Werner syndrome, Dtsch. Zahnaerztl. Z. 25:1026–1029.

    PubMed  CAS  Google Scholar 

  • Friedman, J. M., and Fialkow, P. J., 1976, Cell marker studies of human tumorigenesis, Transplant. Rev. 28:17–33.

    PubMed  CAS  Google Scholar 

  • Fujimoto, W. Y., Green, M. L., and Seegmiller, J. E., 1969, Cockayne’s syndrome: Report of a case with hyperlipoproteinemia, hyperinsulinemia, renal disease, and normal growth hormone, J. Pediatr. 75:881–884.

    PubMed  CAS  Google Scholar 

  • Gabr, M., Hashem, N., Hashem, F., Fahmi, A., and Safouh, M., 1960, Progeria, a pathologic study, J. Pediatr. 57:70–77.

    PubMed  CAS  Google Scholar 

  • Galloway, S. M., and Evans, H. J., 1975, Sister chromatid exchange in human chromosomes from normal individuals and patients with ataxia telangiectasia, Cytogenet. Cell Genet. 15:17–29.

    PubMed  CAS  Google Scholar 

  • Gardner, D. G., and Majka, M., 1969, The early formation of irregular secondary dentine in progeria, Oral Surg. Oral Med. and Oral Pathol. 28:877–884.

    CAS  Google Scholar 

  • Gerald, P. S., 1976, Current concepts in genetics—Sex chromosome disorders, N. Engl. J. Med. 294:706–708.

    PubMed  CAS  Google Scholar 

  • German, J., 1974, Chromosomes and Cancer, John Wiley & Sons, New York.

    Google Scholar 

  • Gershon, D., and Gershon, H., 1976, An evaluation of the “error catastrophe” theory of ageing in the light of recent experimental results, Gerontology 22:212–219.

    PubMed  CAS  Google Scholar 

  • Ghosh, S., and Berry, A. M., 1973, Progeria—A follow up of 8 years, Indian Pediatr. 10:45.

    PubMed  CAS  Google Scholar 

  • Ghosh, S., and Varma, K. P. S., 1964, Progeria: Report of a case with review of the literature, Indian Pediatr. 1:146–155.

    PubMed  CAS  Google Scholar 

  • Giacomini, F., and Rizzi, B., 1968, Considerations on the osteogenic healing process in a case of true progeria, Arch. Ortop. 81:379–389.

    PubMed  CAS  Google Scholar 

  • Gibbs, D. D., 1967, Werner’s syndrome (progeria of the adult), Proc. R. Soc. Med. 60:135–136.

    PubMed  CAS  Google Scholar 

  • Gilford, H., 1897, On the condition of mixed premature and immature development, Trans. Med.-Chir. Soc. Edinburgh 80:17–45.

    CAS  Google Scholar 

  • Gilkes, J. J., Sharvill, D. E., and Wells, R. S., 1974, The premature ageing syndromes: Report of eight cases and description of a new entity named metageria, Br. J. Dermatol. 91:243–262.

    PubMed  CAS  Google Scholar 

  • Ginsberg-Fellner, F., and Knittle, J. L., 1973, Adipose tissue cellularity and metabolism in newly diagnosed juvenile diabetics, Diabetes 22:528–536.

    PubMed  CAS  Google Scholar 

  • Goetz, I., Roberts, E., and Comings, D. E., 1975, Fibroblasts in Huntington’s disease, N. Engl. J. Med. 293:1225–1227.

    PubMed  CAS  Google Scholar 

  • Gold, P., 1971, Antigenic reversion in human cancer, Annu. Rev. Med. 22:85–94.

    PubMed  CAS  Google Scholar 

  • Goldstein, D. E., Drash, A., Gibbs, J., and Blizzard, R. M., 1970, Diabetes mellitus: The incidence of circulating antibodies against thyroid, gastric and adrenal tissue, J. Pediatr. 77:304–306.

    PubMed  CAS  Google Scholar 

  • Goldstein, S., 1969, Lifespan of cultured cells in progeria, Lancet 1:424.

    PubMed  CAS  Google Scholar 

  • Goldstein, S., 1971a, The biology of aging, N. Engl. J. Med. 285: 1120–1129.

    PubMed  CAS  Google Scholar 

  • Goldstein, S., 1971b, On the pathogenesis of diabetes mellitus and its relationship to biological aging, Humangenetik 12: 83.

    PubMed  CAS  Google Scholar 

  • Goldstein, S., 1971c, The role of DNA repair in aging of cultured fibroblasts from Xeroderma pigmentosum and normals, Proc. Soc. Exp. Biol. Med. 137: 730–734.

    CAS  Google Scholar 

  • Goldstein, S., 1978a, Senescence. I. Hormones and aging, in: Metabolic Basis of Endrocrinology (Degroot, Martins, Potts, Nelson, Winegrad, Odell, Steinberger, and Cahill, eds.), Grune and Stratton, New York (in press).

    Google Scholar 

  • Goldstein, S., 19786, Senescence. II. General and cellular aging, in: Metabolic Basis of Endocrinology (Degroot, Martins, Potts, Nelson, Winegrad, Odell, Steinberger, and Cahill, eds.), Grune and Stratton, New York (in press).

    Google Scholar 

  • Goldstein, S., and Moerman, E., 1975a, Heat-labile enzymes in skin fibroblasts from subjects with progeria, N. Engl. J. Med. 292: 1305–1309.

    PubMed  CAS  Google Scholar 

  • Goldstein, S., and Moerman, E. J., 1975b, Heat-labile enzymes in Werner’s syndrome fibroblasts, Nature (London) 255: 159.

    CAS  Google Scholar 

  • Goldstein, S., and Moerman, E. J., 1976a, The Hutchinson—Gilford (progeria) syndrome: Heat-lability of enzymes, in red blood cells in a family, Clin. Res. 24:668A.

    Google Scholar 

  • Goldstein, S., and Moerman, E. J., 1916b, Defective proteins in normal and abnormal human fibroblasts during aging in vitro, Interdiscip. Top. Gerontol. 10: 24–43.

    Google Scholar 

  • Goldstein, S., and Niewiarowski, S., 1976, Increased procoagulant activity in cultured fibroblasts from progeria and Werner’s syndromes of premature ageing, Nature (London) 260:711–713.

    CAS  Google Scholar 

  • Goldstein, S., and Singal, D. P., 1974, Alteration of fibroblast gene products in vitro from a subject with Werner’s syndrome, Nature (London) 251:719–721.

    CAS  Google Scholar 

  • Goldstein, S., and Trieman, G., 1975, Glucose consumption by early and late-passage diploid human fibroblasts during growth and stationary phase, Experientia 31:177–180.

    PubMed  CAS  Google Scholar 

  • Goldstein, S., Littlefield, J. W., and Soeldner, J. S., 1969, Diabetes mellitus and aging: Diminished plating efficiency of cultured human fibroblasts, Proc. Natl. Acad. Sci. U.S.A. 64:155–160.

    PubMed  CAS  Google Scholar 

  • Goldstein, S., Moerman, E. J., Soeldner, J. S., Gleason, R. E., and Barnett, D. M., 1974, Diabetes mellitus and prediabetes: Decreased replicative capacity of cultured fibroblasts, J. Clin. Invest. 53: 27a–27b.

    Google Scholar 

  • Goldstein, S., Niewiarowski, S., and Singal, D. P., 1975, Pathological implications of cell aging in vitro, Fed. Proc. Fed. Am. Soc. Exp. Biol. 34:56–63.

    CAS  Google Scholar 

  • Goldstein, S., Stotland, D., and Cordeiro, R. A. J., 1976, Decreased proteolysis and increased amino acid efflux in aging human fibroblasts. Mech. Agein Dev. 5:221–233.

    CAS  Google Scholar 

  • Goldstein, S., Moerman, E. J., Soeldner, J. S., Gleason, R. E., and Barnett, D. M., 1978, Chronologic age and physiologic status: Effect on replicative lifespan of cultured human fibroblasts from diabetic, prediabetic and normal donors, Science (in press).

    Google Scholar 

  • Good, R. A., and Yunis, E., 1974, Association of autoimmunity, immunodeficiency and aging in man, rabbits and mice, Fed. Proc. Fed. Am. Soc. Exp. Biol. 33:2040–2050.

    CAS  Google Scholar 

  • Gotoff, S. P., Amirmokri, E., and Liebner, E. J., 1967, Ataxia telangiectasia, neoplasia, untoward response to X-irradiation, and tuberous sclerosis, Am. J. Dis. Child. 114:617–625.

    PubMed  CAS  Google Scholar 

  • Gottron, H., 1940, Familiare akrogerie, Arch. Dermatol. Syphilol. 181:571–583.

    Google Scholar 

  • Greene, M. L., Glueck, C. J., Fujimoto, W. Y., and Seegmiller, J. E., 1970, Benign symmetric lipomatosis (Launois-Bensaude adenolipomatosis) with gout and hyperlipoproteinemia, Am. J. Med. 48: 239–246.

    PubMed  CAS  Google Scholar 

  • Griffin, J. E., Punyashthiti, K., and Wilson, J. D., 1976, Dihydrotestosterone binding by cultured human fibroblasts: Comparison of cells from control subjects and from patients with hereditary male pseudohermaphroditism due to androgen resistance, J. Clin. Invest. 57:1342–1351.

    PubMed  CAS  Google Scholar 

  • Grunebaum, M., 1973, Progeria, Postgrad. Med. 53:221–222.

    PubMed  CAS  Google Scholar 

  • Gsell, O., and Haensch, G., 1971, Werner’s syndrome: A case report on premature aging, Schweiz. Med. Wochenschr. 101:418–421.

    PubMed  CAS  Google Scholar 

  • Haerer, A. F., Jackson, J. F., and Evers, C. G., 1969, Ataxia-telangiectasia with gastric adenocarcinoma, J. Am. Med. Assoc. 210:1884–1887.

    CAS  Google Scholar 

  • Hall, B. D., Berg, B. O., Rudolph, R. S., and Epstein, C. J., 1974, Pseudoprogeria-Hallermann-Streiff (PHS) syndrome, Birth Defects: Orig. Artic. Ser. 10:137–146.

    CAS  Google Scholar 

  • Hamlin, C. R., Kohn, R. R., and Luschin, J. H., 1975, Apparent accelerated aging of human collagen in diabetes mellitus, Diabetes 24:902–904.

    PubMed  CAS  Google Scholar 

  • Harnden, D. G., 1974, Ataxia telangiectasia syndrome: Cytogenetic and cancer aspects, in: Chromosomes and Cancer (J. German, ed.), pp. 619–636, John Wiley & Sons, New York.

    Google Scholar 

  • Hart, R. W., and Trosko, J. E., 1976, DNA repair processes in mammals, Interdiscip. Top. Gerontol. 9:134–167.

    CAS  Google Scholar 

  • Haslam, R. J., and Goldstein, S., 1974, Adenosine 3′:5′-cyclic monophosphate in young and senescent human fibroblasts during growth and stationary phase in vitro: Effects of prostaglandin E1 and of adrenaline, Biochem. J. 144:253–263.

    PubMed  CAS  Google Scholar 

  • Hassell, T. M., Page, R. C., Narayanan, S., and Cooper, C. G., 1976, Diphenylhydantoin (Dilantin) gingival hyperplasia: Drug-induced abnormality of connective tissue, Proc. Natl. Acad. Sci. U.S.A. 73:2909–2912.

    PubMed  CAS  Google Scholar 

  • Hayflick, L., 1965, The limited in vitro lifetime of human diploid cell strains, Exp. Cell Res. 37:614–636.

    PubMed  CAS  Google Scholar 

  • Hecht, F., Koler, R. D., Rigas, D. A., Dahnke, G. S., Case, M. P., Tisdale, V., and Miller, R. W., 1966, Leukemia and lymphocytes in ataxia-telangiectasia, Lancet 2:1193.

    Google Scholar 

  • Hecht, F., McCaw, B. K., and Koler, R. D., 1973, Ataxia-telangiectasia-Clonal growth of translocation lymphocytes, N. Engl. J. Med. 289:286–291.

    PubMed  CAS  Google Scholar 

  • Hernandez, A. L., DeLeon, B., Garcia de la Puenti, S., and Del Castillo, V., 1975, Ultrastructural renal lesions in the Cockayne syndrome: A case report, Rev. Invest. Clin. 27:153–158.

    PubMed  CAS  Google Scholar 

  • Higurashi, M., and Conen, P. E., 1973, In vitro chromosomal radiosensitivity in chromosomal breakage syndromes, Cancer 32:380–383.

    PubMed  CAS  Google Scholar 

  • Hoar, D. I., 1975, Phenotypic manifestations of ataxia-telangiectasia, Lancet 2:1048.

    PubMed  CAS  Google Scholar 

  • Hoar, D. I., and Sargent, P., 1976, Chemical mutagen hypersensitivity in ataxia-telangiectasia, Nature (London) 261:590–592.

    CAS  Google Scholar 

  • Holliday, R., Porterfield, J. S., and Gibbs, D. D., 1974, Premature ageing and occurrence of altered enzyme in Werner’s syndrome fibroblasts, Nature (London) 248:762–763.

    CAS  Google Scholar 

  • Hopkins, D. J., and Horan, E. C., 1970, Glaucoma in the Hallermann-Streiff syndrome, Br. J. Ophthalmol. 54:416–422.

    PubMed  CAS  Google Scholar 

  • Hoppe, W., and Koritsch, H. D., 1972, Another case of meningioma in a patient with Werner’s syndrome, Psychiatr. Neurol. Med. Psychol. 24:611–617.

    CAS  Google Scholar 

  • Howell, T. H., 1975, Old Age, p. 115, H. K. Lewis, London.

    Google Scholar 

  • Huang, K.-E., 1975, Pituitary response to synthetic luteinizing hormone-releasing hormone in patients with Turner’s syndrome, J. Clin. Endocrinol. Metab. 41:771–776.

    PubMed  CAS  Google Scholar 

  • Huang, S.-W., and Maclaren, N. K., 1976, Insulin-dependent diabetes: A disease of autoaggression, Science 192:64–66.

    PubMed  CAS  Google Scholar 

  • Hutchinson, D., 1971, Oral manifestations of oculomandibulodyscephaly with hypotrichosis (Hallermann-Streiff syndrome), Oral Surg. Oral Med. Oral Pathol. 31:234–244.

    PubMed  CAS  Google Scholar 

  • Hutchinson, J., 1886, Congenital absence of hair and mammary glands, Trans. Med.-Chir. Soc. Edinburgh 69:473–477.

    CAS  Google Scholar 

  • Ishii, T., 1976, Progeria: Autopsy report of one case, with a review of pathologic findings reported in the literature, J. Am. Geriatr. Soc. 24:193–202.

    PubMed  CAS  Google Scholar 

  • Ishii, T., and Hosoda, Y., 1974, Autopsy of Werner’s syndrome, Jpn. J. Geriatr. 11:408–415.

    CAS  Google Scholar 

  • Ishii, T., and Hosoda, Y., 1975, Werner’s syndrome: Autopsy report of one case, with a review of pathologic findings reported in the literature, J. Am. Geriatr. Soc. 23:145–154.

    PubMed  CAS  Google Scholar 

  • Jervis, G. A., 1970, Premature senility in Down’s syndrome, Ann. N. Y. Acad. Sci. 171:559–561.

    Google Scholar 

  • Johansen, K. Soeldner, J. S., Gleason, R. E., Gottlieb, M. S., Park, B. N., Kaufmann, R. L., and Tan, M. H., 1975, Serum insulin and growth hormone response patterns in monozygotic twin siblings of patients with juvenile-onset diabetes, N. Engl. J. Med. 293:57–61.

    PubMed  CAS  Google Scholar 

  • Jones, K. L., Smith, D. W., Harvey, M. A., Hall, B. D., and Quan, L., 1975, Older paterna age and fresh gene mutation: Data on additional disorders, J. Pediatr. 86:84–88.

    PubMed  CAS  Google Scholar 

  • Kaiman, H., Lambie, R. W., and Metzl, 1969, Progeria: Case description, Clin. Pediatr. (Philadelphia) 8:411–415.

    CAS  Google Scholar 

  • Kato, H., and Stich, H. F., 1976, Sister chromatid exchanges in aging and repair-dehcient human fibroblasts, Nature (London) 260:447–448.

    CAS  Google Scholar 

  • Kaufman, M., Straisfeld, C., and Pinsky, L., 1977, Expression of androgen-responsive properties in human skin fibroblast strains of genital and nongenital origin, Somat. Cell Genet. 3:17–25.

    PubMed  CAS  Google Scholar 

  • Keay, A. J., Oliver, M. F., and Boyd, G. S., 1955, Progeria and atherosclerosis, Arch. Dis. Child. 30:410–414.

    PubMed  CAS  Google Scholar 

  • Kidd, R. L., and Wilgram, G. F., 1972, Morphea and progeria, Arch. Dermatol. 105:770–771.

    PubMed  CAS  Google Scholar 

  • Kohn, R. R., 1975, Aging and cell division, Science 188:203–204.

    PubMed  CAS  Google Scholar 

  • Korein, J., Steinman, P. A., and Senz, E. H., 1961, Ataxia-telangiectasia: Report of a case and review of the literature, Arch. Neurol. 4:272–280.

    PubMed  CAS  Google Scholar 

  • Kraus, B. S., Gottlieb, M. A., and Meliton, H. R., 1970, The dentition in Rothmund’s syndrome, J. Am. Dent. Assoc. 81:895–915.

    PubMed  CAS  Google Scholar 

  • Kristensen, J. K., 1975, Poikiloderma congénitale—An early case of Rothmund-Thomson’s syndrome, Ada Derm.-Venereol. 55:316–318.

    CAS  Google Scholar 

  • Kulenkamp, D., Scholz-Kordan, D., Passarge, E., Rudiger, H. W., and Ruprecht, K. W., 1973, Werner’s syndrome: A hereditable disorder of multiple organ systems, Andrologie 5:299–310.

    PubMed  CAS  Google Scholar 

  • Kvale, P. A., Rutt, W. M., Birk, R. E., and Eyler, W. R., 1965, Werner’s syndrome, Henry Ford Hosp. Med. J. 13:411–420.

    PubMed  CAS  Google Scholar 

  • Land, V. J., and Nogrady, M. B., 1969, Cockayne’s syndrome, J. Can. Assoc. Radiol. 20:194–203.

    PubMed  CAS  Google Scholar 

  • Lanning, M., and Simil, A. S., 1970, Cockayne’s syndrome: Report of a case with normal intelligence, Z. Kinderheilkd. 109:70–75.

    PubMed  CAS  Google Scholar 

  • Larregue, M., Cathelineau, G., Binet, O., Lhullier, N., Timsit, E., and Graciansky, P. De, 1974, Werner’s syndrome and hyperinsulinic diabetes, Ann. Dermatol. Syphiligr. 101:135–144.

    CAS  Google Scholar 

  • Latt, S. A., Stetten, G. M., Juergens, L. A., Buchanan, G. R., and Gerald, P. S., 1975, Induction by alklyating agents of sister chromatid exchanges and chromatid breaks in Fanconi’s anemia, Proc. Natl. Acad. Sci. U.S.A. 72:4066–4070.

    PubMed  CAS  Google Scholar 

  • Leaf, A., 1973, Unusual longevity: The common denominator, Hosp. Pract. 8:79–86.

    Google Scholar 

  • Le Guilly, Y., Simon, M., Lenoir, P., and Bourel, M., 1973, Long-term culture of human adult liver cells: Morphological changes related to in vitro senescence and effect of donor’s age on growth potential, Gerontologia 19:303–313.

    PubMed  Google Scholar 

  • Lelis, I. I., 1975, Progeria of adults (Werner’s syndrome) Ter. Arkh. 47(1):99–102.

    PubMed  CAS  Google Scholar 

  • Lenz, W. D., and Majewski, F., 1974, A generalized disorder of the connective tissues with progeria, choanal atresia, symphalangism, hypoplasia of dentine and craniodiaphyseal hypostosis, Birth Defects: Orig. Artic. Ser. 10:133–136.

    CAS  Google Scholar 

  • Lestradet, H., Deschamps, I., and Giron, B., 1976, Insulin and free fatty acid levels during oral glucose tolerance tests and their relation to age in 70 healthy children, Diabetes 25:505–508.

    PubMed  CAS  Google Scholar 

  • Levin, S., and Perlov, S., 1971, Ataxia-telangiectasia in Israel, with observations on its relationship to malignant disease, Isr. J. Med. Sci. 7:1535–1541.

    PubMed  CAS  Google Scholar 

  • Levine, M. D., Alexander, E., and Rimoin, D. L., 1975, Progeroid syndrome, Birth Defects: Orig. Artie. Ser. 11:308–309.

    CAS  Google Scholar 

  • Lewis, M. B., 1972, Rothmund-Thomson syndrome and fibrocystic disease, Australas. J. Dermatol. 13:105–106.

    PubMed  CAS  Google Scholar 

  • Lieberman, M. W., 1976, Approaches to the analysis of fidelity of DNA repair in mammalian cells, Int. Rev. Cytol. 45:1–23.

    PubMed  CAS  Google Scholar 

  • Like, A. A., and Rossini, A. A., 1976, Streptozotocin-induced pancreatic insulitis: A new model of diabetes mellitus, Science 193:415–417.

    PubMed  CAS  Google Scholar 

  • Lindeman, R. D., 1975, Age changes in renal function, in: The Physiology and Pathology of Human Aging (R. Goldman and M. Rockstein, eds.), pp. 19–38, Academic Press, New York.

    Google Scholar 

  • Lindsten, J., 1963, in: The Nature and Origin of X Chromosome Aberrations in Turner’s Syndrome (Almquist and Wiksell, eds.), Stockholm.

    Google Scholar 

  • Lindsten, J., Cerasi, E., Luft, R., and Hultquist, G., 1967, The occurrence of abnormal insulin and growth hormone (HGH) responses to sustained hyperglycaemia in a disease with sex chromosome aberrations (Turner’s syndrome): Including a histological study of the pancreas in two such patients, Acta Endocrinol.(Copenhagen) 56: 107–131.

    CAS  Google Scholar 

  • Linn, S., Kairis, M., and Holliday, R., 1976, Decreased fidelity of DNA polymerase activity isolated from aging human fibroblasts, Proc. Natl. Acad. Sci. U.S.A. 73:2818–2822.

    PubMed  CAS  Google Scholar 

  • Lisker, R., and Cobo, A., 1970, Chromosome breakage in ataxia-telangiectasia, Lancet 1:618.

    PubMed  CAS  Google Scholar 

  • Little, J. B., Epstein, J., and Williams, J. R., 1975, Repair of DNA strand breaks in progeric fibroblasts and aging human diploid cells, Basic Life Sci. 58:793–800.

    Google Scholar 

  • Lodi, A., Ravaglia, G., Grigioni, F., Ravaioli, R., and Gritti, F., 1974, Endocrine and morphological aspects of Werner’s syndrome, J. Clin. Med. 55:652–674.

    CAS  Google Scholar 

  • Louis-Bar, D., 1941, Sur un syndrome progressif comprenant des télangiectasies capillaires cutanées et conjonctivales, à disposition naevoïde et des troubles cérébelleux, Confin. Neurol. 4:32–42.

    Google Scholar 

  • MacDonald, W. B., Fitch, K. D., and Lewis, I. C., 1960, Cockayne’s syndrome: A heredo-familial disorder of growth and development, Pediatrics 25:997–1007.

    PubMed  CAS  Google Scholar 

  • Macleod, W., 1966, Progeria, Br. J. Radiol. 39:224–226.

    PubMed  CAS  Google Scholar 

  • MacNamara, B. G., Farn, K. T., Mitra, A. K., Lloyd, J. K., and Fosbrooke, A. S., 1970, Progeria: Case report with long-term studies of serum lipids, Arch. Dis. Child. 45:553–560.

    PubMed  CAS  Google Scholar 

  • Malamud, N., 1972, Neuropathology of organic brain syndromes associated with aging, in: Aging and the Brain (CM. Gaitz, ed.), pp. 63–87, Plenum Press, New York.

    Google Scholar 

  • Marble, A., and Ramos, E., 1971, Cancer and diabetes, in: Joslin’s Diabetes Mellitus (A. Marble, P. White, R. F. Bradley, and L. P. Krall, eds.), pp. 695–700, Lea & Febiger, Philadelphia.

    Google Scholar 

  • Marcondes, E., Campos, J. V., Barbieri, D., Quarentei, G., and Cavallo, A., 1969, Progeria: Case report with progressive systemic sclerotic manifestations since birth, Rev. Hosp. Clin. Fac. Med. Univ. Sao Paulo 24:147–154.

    CAS  Google Scholar 

  • Margolin, F. R., and Steinbach, H. L., 1968, Progeria: Hutchinson-Gilford syndrome, Am. J. Roentgenol. Radium Ther. Nucl. Med. 103:173–178.

    PubMed  CAS  Google Scholar 

  • Marks, H. H., and Krall, L. P., 1971, Onset, course, prognosis and mortality in diabetes mellitus, in: Joslin’s Diabetes Mellitus (A. Marble, P. White, R. F. Bradley, and L. P. Krall, eds.), pp. 209–254, Lea & Febiger, Philadelphia.

    Google Scholar 

  • Martin, G. M., 1977, Genetic syndromes in man with potential relevance to the pathobiology of aging, in: Genetic Effects on Aging, Birth Defects: Orig. Artic. Ser. (D. Bergsma and D. E. Harrison, eds.) The National Foundation-March of Dimes, New York (in press).

    Google Scholar 

  • Martin, G. M., Sprague, CA., and Epstein, C.J., 1970, Replicative life-span of cultivated human cells: Effects of donor’s age, tissue, and genotype, Lab. Invest. 23:86–92.

    PubMed  CAS  Google Scholar 

  • Martin, G. M., Sprague, C. A., Norwood, T. H., and Pendergrass, W. R., 1974, Clonal selection, attenuation and differentiation in an in vitro model of hyperplasia, Am. J. Pathol. 74:137–154.

    PubMed  CAS  Google Scholar 

  • Martin, J. J., Deberot, R., Philippart, M., Van Acker, K. J., and Hooft, C., 1971, Peculiar dysmorphic syndrome with orthochromatic leucodystrophy: Discussion of its relationship with Cockayne’s syndrome and Pelizaeus-Merzbacher’s disease, Acta Neuropathol. 18:224–233.

    PubMed  CAS  Google Scholar 

  • Maurer, R. M., and Langford, O. L., 1967, Rothmund’s syndrome: A cause of résorption of phalangeal tufts and dystrophic calcification, Radiology 89:706–708.

    PubMed  CAS  Google Scholar 

  • McCaw, B. K., Hecht, F., Harnden, D. G., and Teplitz, R. L., 1975, Somatic rearrangement of chromosome 14 in human lymphocytes, Proc. Natl. Acad. Sci. U.S.A. 72:2071–2075.

    PubMed  CAS  Google Scholar 

  • McFarlin, D. W., Strober, W., and Waldmann, T. A., 1972, Ataxia telangiectasia, Medicine (Baltimore) 51:281–314.

    CAS  Google Scholar 

  • McKusick, V. A., 1963, Medical genetics, 1962, J. Chronic Dis. 16:457–634.

    PubMed  CAS  Google Scholar 

  • McKusick, V. A., 1975, Mendelian Inheritance in Man—Catalogs of Autosomal Dominant, Autosomal Recessive and X-Linked Phenotypes, Johns Hopkins University Press, Baltimore.

    Google Scholar 

  • McKusick, V. A., and Cross, H. E., 1966, Ataxia-telangiectasia and Swiss-type agammaglobulinemia: Two genetic disorders of the immune mechanism in related Amish sibships, J. Am. Med. Assoc. 195:739–745.

    CAS  Google Scholar 

  • Meissner, W. A., and Legg, M. A., 1971, The pathology of diabetes, in: Joslin’s Diabetes Mellitus (A. Marble, P. White, R. F. Bradley, and L. P. Krall, eds.), pp. 157–190, Lea & Febiger, Philadelphia.

    Google Scholar 

  • Menkes, J. H., and Stein, N., 1973, Fibroblast cultures in Huntington’s disease, N. Engl. J. Med. 288:856–857.

    PubMed  CAS  Google Scholar 

  • Miller, M. E., and Chatten, J., 1967, Ovarian changes in ataxia telangiectasia, Acta Paediatr. Scand. 56:559–561.

    PubMed  CAS  Google Scholar 

  • Miller, R. W., 1970, Neoplasia and Down’s syndrome, Ann. N. Y. Acad. Sci. 171:637–644.

    Google Scholar 

  • Moosa, A., and Dubowitz, V., 1970, Peripheral neuropathy in Cockayne’s syndrome, Arch. Dis. Child. 45:674–677.

    PubMed  CAS  Google Scholar 

  • Moossey, J., 1967, The neuropathology of Cockayne’s syndrome, J. Neuropathol. Exp. Neurol. 26:654–660.

    Google Scholar 

  • Morgan, J. L., Holcomb, T. M., and Morrissey, R. W., 1968, Radiation reaction in ataxia telangiectasia, Am. J. Dis. Child. 116:577–558.

    Google Scholar 

  • Morse, L. S., and Pauling, C., 1975, Induction of error-prone repair as a consequence of DNA ligase deficiency in E. coli, Proc. Natl. Acad. Sci. U.S.A. 72:4645–4649.

    CAS  Google Scholar 

  • Mostafa, A. H., and Gabr, M., 1954, Heredity in progeria: With follow-up of two affected sisters, Arch. Pediatr. 71:163–172.

    PubMed  CAS  Google Scholar 

  • Muller, J., Kunkov, A. A., and Kepertov, A. A., 1969, Werner’s syndrome: Case report, Wien. Z. Inn. Med. Ihre Grenzgeb. 50:112–116.

    CAS  Google Scholar 

  • Murphy, R., and Achkar, E. J., 1966, Werner’s syndrome, Lahey Clin. Found. Bull. 15: 1–7.

    PubMed  CAS  Google Scholar 

  • Neill, C. A., and Dingwall, M. M., 1950, A syndrome resembling progeria: A review of two cases, Arch. Dis. Child. 25: 213–223.

    PubMed  CAS  Google Scholar 

  • Nelson, P. G., Pyke, D. A., Cudworth, A. G., Woodrow, J. C., and Batchelor, J. R., 1975, Histocompatibility antigens in diabetic identical twins, Lancet 2:193–194.

    PubMed  CAS  Google Scholar 

  • Neufeld, E. F., Lim, T. W., and Shapiro, L. J., 1975, Inherited disorders of lysosomal metabolism, Annu. Rev. Biochem. 44:357–376.

    PubMed  CAS  Google Scholar 

  • Nielsen, J., Johansen, K., and Yde, H., 1969, The frequency of diabetes mellitus in patients with Turner’s syndrome and pure gonadal dysgenesis, Acta Endocrinol. (Copenhagen) 62:251–269.

    CAS  Google Scholar 

  • Nienhaus, A. J., De Jong, B., and Kate, L. P. Ten, 1971, Fibroblast culture in Werner’s syndrome, Humangenetik 13:244–246.

    PubMed  CAS  Google Scholar 

  • Nissim, J. E., 1971, Rothmund syndrome, Birth Defects: Orig. Artie. Ser. 7:294–295.

    CAS  Google Scholar 

  • Norman, R. M., and Tingey, A. H., 1966, Syndrome of micrencephaly, strio-cerebellar calcifications and leucodystrophy, J. Neurol. Neurosurg. Psychiatry 29:157–163.

    Google Scholar 

  • Nowell, P. C., 1976, The clonal evolution of tumor cell populations: Acquired genetic lability permits stepwise selection of variant sublines and underlies tumor progression, Science 194:23–28.

    PubMed  CAS  Google Scholar 

  • Oates, R. K., Lewis, M. B., and Walker-Smith, J. A., 1971, The Rothmund-Thomson syndrome: Case report of an unusual syndrome, Aust. Paediatr. J. 7:103–107.

    PubMed  CAS  Google Scholar 

  • Ohno, T., and Hiroaka, M., 1966, Renal lesions in Cockayne’s syndrome, Tohoku J. Exp. Med. 89:151–166.

    PubMed  CAS  Google Scholar 

  • Orgel, L. E., 1973, Ageing of clones of mammalian cells, Nature (London) 243: 441–445.

    CAS  Google Scholar 

  • Oxford, J. M., Harnden, D. G., Parrington, J. M., and Delhanty, J. D., 1975, Specific chromosome aberrations in ataxia telangiectasia, J. Med. Genet. 12:251–262.

    PubMed  CAS  Google Scholar 

  • Ozonoff, M. B., and Clemett, A. R., 1967, Progressive osteolysis in progeria, Am. J. Roentgenol. Radium Ther. Nucl. Med. 100:75–79.

    PubMed  CAS  Google Scholar 

  • Paddison, R. M., Moossy, J., Derbes, V. J., and Kloepfer, H. W., 1963, Cockayne’s syndrome: A report of five new cases with biochemical, chromosomal, dermatologie, genetic and neuropathologic observations, Dermatol. Trop. Ecol. Geogr. 2:195–203.

    Google Scholar 

  • Palmer, G., 1966, Rothmund-Thomson syndrome, Australas. J. Dermatol. 8:253–254.

    CAS  Google Scholar 

  • Palumbo, P. J., Elveback, L. R., Chu, C.-P., Connolly, D. C., and Kurland, L. T., 1976, Diabetes mellitus: Incidence, prevalence, survivorship, and causes of death in Rochester, Minnesota, 1945-1970, Diabetes 25:566–573.

    PubMed  CAS  Google Scholar 

  • Paterson, D., 1922, Case of progeria, Proc. R. Soc. Med. 16:42.

    Google Scholar 

  • Paterson, M. C., Smith, B. P., Lohman, P. H. M., Anderson, A. K., and Fishman, L., 1976, Defective excision repair of ϒ-ray-damaged DNA in human (ataxia telangiectasia) fibroblasts, Nature (London) 260:444–447.

    CAS  Google Scholar 

  • Payer, G., 1969, Two cases of Werner’s syndrome, Klin. Monatsbl. Augenheilkd. 155:901–904.

    PubMed  CAS  Google Scholar 

  • Penrose, L. S., and Smith, G. F., 1966, Down’s Anomaly, Churchill, London.

    Google Scholar 

  • Perlman, H. H., Luscombe, H. A., and Rosenberg, P. E., 1967, Poikiloderma congénitale of Thomson-Rothmund vs. localized linear scleroderma, Arch. Dermatol. 96:593–594.

    PubMed  CAS  Google Scholar 

  • Perry, R. P., 1976, Processing of RNA, Annu. Rev. Biochem. 45:605–630.

    PubMed  CAS  Google Scholar 

  • Peterson, R. D. A., Kelly, W. D., and Good, R. A., 1964, Ataxia-telangiectasia: Its association with a defective thymus, immunological-deficiency disease and malignancy, Lancet 1:1189–1193.

    PubMed  CAS  Google Scholar 

  • Peterson, R. D. A., Cooper, M. D., and Good, R. A., 1966, Lymphoid tissue abnormalities associated with ataxia-telangiectasia, Am. J. Med. 41:342–359.

    PubMed  CAS  Google Scholar 

  • Pfeiffer, R. A., and Backmann, K. D., 1973, An atypical case of Cockayne’s syndrome, Clin. Genet. 4:28–32.

    PubMed  CAS  Google Scholar 

  • Piazzini, M., Conti, C., Guazzelli, R., and Bigozzi, U., 1976, On a rare case of progeria in brother and sister, Acta Med. Auxol. 8:75–79.

    Google Scholar 

  • Poon, P. K., O’Brien, R. L., and Parker, J. W., 1974, Defective DNA repair in Fanconi’s anaemia, Nature (London) 250:223–225.

    CAS  Google Scholar 

  • Predescu, V., Christodorescu, D., Coltoiu, A., Costiner, E., Hagiopol, V., and Alexianu, M., 1973, Cockayne’s syndrome, Arch. Fr. Pediatr. 30:527–532.

    PubMed  CAS  Google Scholar 

  • Rainbow, A. J., and Howes, M., 1977, Decreased repair of gamma ray damaged DNA in progeria, Biochem. Biophys. Res. Commun. 77:714–719.

    Google Scholar 

  • Rary, J. M., Bender, M. A., and Kelly, T. E., 1975, A 14/14 marker chromosome lymphocyte clone in ataxia telangiectasia, J. Hered. 66:33–35.

    PubMed  CAS  Google Scholar 

  • Rasio, E., Antaki, A., and Van Campenhout, J., 1976, Diabetes mellitus in gonadal dysgenesis: Studies of insulin and growth hormone secretion, Eur. J. Clin. Invest. 6:59–66.

    PubMed  CAS  Google Scholar 

  • Rava, G., 1967, Su un nucleo familiare di progeria, Minerva Med. 58:1502–1509.

    PubMed  CAS  Google Scholar 

  • Regan, J. D., and Setlow, R. B., 1974, DNA repair in human progeroid cells, Biochem. Biophys. Res. Common. 59:858–864.

    CAS  Google Scholar 

  • Reichel, W., and Garcia-Bunuel, R., 1970, Pathologic findings in progeria: Myocardial fibrosis and lipofuscin pigment, Am. J. Clin. Pathol. 53:243–253.

    PubMed  CAS  Google Scholar 

  • Reichel, W., Garcia-Bunuel, R., and Dilallo, J., 1971a, Progeria and Werner’s syndrome as models for the study of normal human aging, J. Am. Geriatr. Soc. 19: 369–375.

    PubMed  CAS  Google Scholar 

  • Reichel, W., Bailey, J. A., Zigel, S., Garcia-Bunuel, R., and Knox, G., 1971b, Radiological findings in progeria, J. Am. Geriatr. Soc. 19:657–674.

    PubMed  CAS  Google Scholar 

  • Reiss, U., and Gershon, D., 1976, Rat liver Superoxide dismutase: Purification and age-related modifications, Eur. J. Biochem. 63:617–623.

    PubMed  CAS  Google Scholar 

  • Remsen, J. F., and Cerutti, P. A., 1976, Deficiency of gamma-ray excision repair in skin fibroblasts from Fanconi’s anemia, Proc. Natl. Acad. Sci. U.S.A. 73:2419–2423.

    PubMed  CAS  Google Scholar 

  • Renold, A. E., Stauffacher, W., and Cahill, G. F. Jr., 1972, Diabetes mellitus, in: The Metabolic Bases of Inherited Disease (J. B. Stanbury, J. B. Wyngaarden, and D. S. Fredrickson, eds.), pp. 83–118, McGraw-Hill, New York.

    Google Scholar 

  • Reye, C., and Mosman, N. S. W., 1960, Ataxia-telangiectasia, Am. J. Dis. Child. 99:238–247.

    Google Scholar 

  • Reynolds, C., O’Duffy, J. D., and Sams, W., 1972, Werner’s syndrome: Case report of a variant, Minn. Med. 55:917–921.

    PubMed  CAS  Google Scholar 

  • Rheinwald, J. G., and Green, H., 1975, Serial cultivation of strains of human epidermal keratinocytes: The formation of keratinizing colonies from single cells, Cell 6:331–337.

    PubMed  CAS  Google Scholar 

  • Richards, D., 1974, Werner’s syndrome, Proc. R. Soc. Med. 67:721–722.

    Google Scholar 

  • Riggs, W., and Seibert, J., 1972, Cockayne’s syndrome: Roentgen findings, Am. J. Roentgenol. Radium Ther. Nucl. Med. 116:623–633.

    PubMed  Google Scholar 

  • Rosen, R. S., Cimini, R., and Coblentz, D., 1970, Werner’s syndrome, Br. J. Radiol. 43:193–198.

    PubMed  CAS  Google Scholar 

  • Rosenbloom, A. L., and Debusk, F. L., 1971, Progeria of Hutchinson-Gilford: A caricature of aging, Am. Heart J. 83:287–289.

    Google Scholar 

  • Rosenbloom, A. L., Karacan, I. J., and DeBusk, F. L., 1970, Sleep characteristics and endocrine response in progeria, J. Pediatr. 77:692–695.

    PubMed  CAS  Google Scholar 

  • Rosenbloom, A. L., Wheeler, L., Bianchi, R., Chin, F. T., Tiwary, C. M., and Grgic, A., 1975, Age-adjusted analysis of insulin responses during normal and abnormal glucose tolerance tests in children and adolescents, Diabetes 24:820–828.

    PubMed  CAS  Google Scholar 

  • Rosenbloom, A. L., Goldstein, S., and Yip, C. C., 1976, Insulin binding to cultured human fibroblasts increases with normal and precocious aging, Science 193:412–415.

    PubMed  CAS  Google Scholar 

  • Rothmund, A., 1868, Über Kataracten in Verbindung mit einer eigenthen Haut Degeneration, Graefe. Arch. Ophthalmol. 14:159–182.

    Google Scholar 

  • Rothstein, M., 1977, Recent developments in the age-related alteration of enzymes: A review, Mech. Ageing Dev. 6:241–257.

    PubMed  CAS  Google Scholar 

  • Rowe, J. W., Andres, R., Tobin, J. D., Norrs, A. H., and Shock, N. W., 1976, The effect of age on creatinine clearance in man: A cross-sectional and longitudinal study, J. Gerontol. 31:155–163.

    PubMed  CAS  Google Scholar 

  • Rowlatt, U., 1969, Cockayne’s syndrome: Report of case with necropsy findings, Acta Neuropathol. 14:52–61.

    PubMed  CAS  Google Scholar 

  • Roy, S., Srivastava, R. N., Gupta, P. C., and Mayekar, G., 1973, Ultrastructure of peripheral nerve in Cockayne’s syndrome, Acta Neuropathol. 24:345–349.

    PubMed  CAS  Google Scholar 

  • Roychoudhury, D. S., and Banerjee, A. K., 1968, Heredofamilial study of Weber-Cockayne disease, Bull. Calcutta Sch. Trop. Med. 16:12–13.

    PubMed  CAS  Google Scholar 

  • Rubin, P., and Casarett, G. W., 1968, Clinical Radiation Pathology, pp. 881–893, W. B. Saunders Co., Philadelphia.

    Google Scholar 

  • Ruddle, F. H., and Creagan, R. P., 1975, Parasexual approaches to the genetics of man, Annu. Rev. Genet. 9:407–486.

    PubMed  CAS  Google Scholar 

  • Ryan, J. M., and Cristofalo, V. J., 1975, Chromatin template activity during aging in vitro, Exp. Cell Res. 90:456–458.

    PubMed  CAS  Google Scholar 

  • Saunders, J. W., and Fallon, J. F., 1966, Cell death in morphogenesis, in: Major Problems in Developmental Biology (M. Locke, ed.), pp. 289–314, Academic Press, New York.

    Google Scholar 

  • Schalch, D. S., McFarlin, D., and Barlow, M. H., 1970, An unusual form of diabetes mellitus in ataxia telangiectasia, N. Engl. J. Med. 282:1396–1402.

    PubMed  CAS  Google Scholar 

  • Schmickel, R. D., Chu, E. H. Y., and Trosko, J., 1975, The definition of a cellular defect in two patients with Cockayne syndrome, Pediatr. Res. 9: 317 (abstract).

    Google Scholar 

  • Schneider, E. L., and Chase, G. A., 1976, Relationship between age of donor and in vitro life span of human diploid fibroblasts, Interdiscip. Top. Gerontol. 10:62–69.

    Google Scholar 

  • Schneider, E. L., and Epstein, C. J., 1972, Replication rate and lifespan of cultured fibroblasts in Down’s syndrome, Proc. Soc. Exp. Biol. Med. 141:1092–1096.

    PubMed  CAS  Google Scholar 

  • Schneider, E. L., and Mitsui, Y., 1976, The relationship between in vitro cellular aging and in vivo human age, Proc. Natl. Acad. Sci. U.S.A. 73:3584–3588.

    PubMed  CAS  Google Scholar 

  • Schneider, E. L., and Shorr, S. S., 1975, Alteration in cellular RNA’s during the in vitro lifespan of cultured human diploid fibroblasts, Cell 6:179–184.

    PubMed  CAS  Google Scholar 

  • Schumacher, K., Rodermund, O. E., and Doepfmer, R., 1969, Werner’s syndrome: Contribution to symptomatology and etiology, Arch. Klin. Med. 216:116–147.

    PubMed  CAS  Google Scholar 

  • Segal, D. J., and McCoy, E. E., 1974, Studies on Down’s syndrome in tissue culture. I. Growth rates and protein contents of fibroblast cultures, J. Cell. Physiol. 83:85–90.

    PubMed  CAS  Google Scholar 

  • Sexton, G. B., 1954, Thomson’s syndrome (poikiloderma congénitale), Can. Med. Assoc. J. 70:662–665.

    PubMed  CAS  Google Scholar 

  • Shuster, J., Hart, Z., Stimson, C. W., Brough, A. J., and Poulik, M. D., 1966, Ataxiatelangiectasia with cerebellar tumor, Pediatrics 37:776–786.

    PubMed  CAS  Google Scholar 

  • Siemens, H. W., 1963, The lens, in: Genetics and Ophthalmology (P. J. Waardenburg, A. Franceschetti, and D. Klein, eds.), p. 896, Charles C. Thomas, Springfield, Illinois. Silver, H. K., 1966, Rothmund-Thomson syndrome: An oculocutaneous disorder, Am. J. Dis. Child. 111:182–190.

    Google Scholar 

  • Simig, I., and Fizelov, A. E., 1976, Werner’s syndrome, Cesk. Oftalmol. 32:45–49.

    PubMed  CAS  Google Scholar 

  • Singal, D. P., and Blajchman, M. A., 1973, Histocompatibility (HL-A) antigens, lymphocytotoxic antibodies and tissue antibodies in patients with diabetes mellitus, Diabetes 22:429–432.

    PubMed  CAS  Google Scholar 

  • Singal, D. P., and Goldstein, S., 1973, Absence of detectable HL-A antigens on cultured fibroblasts in progeria, J. Clin. Invest. 52:2259–2263.

    PubMed  CAS  Google Scholar 

  • Smith, D. W., 1976, Ataxia-telangiectasia syndrome in: Recognizable Patterns of Human Malformation, pp. 102–103, W. B. Saunders Co., Philadelphia.

    Google Scholar 

  • Smith, G. F., and Berg, J. M., 1976, Down’s Anomaly, pp. 239–246, Churchill Livingstone, Edinburgh.

    Google Scholar 

  • Sourander, P., Bonnevier, J. O., and Olsson, Y., 1966, A case of ataxia telangiectasia with lesions in the spinal cord, Acta Neurol. Scand. 42:354–366.

    PubMed  CAS  Google Scholar 

  • Spark, H., 1965, Cachetic dwarfism resembling the Cockayne-Neill type, J. Pediatr. 66:41–47.

    PubMed  CAS  Google Scholar 

  • Spence, A. M., and Herman, M. M., 1973, Critical re-examination of the premature aging concept in progeria: A light and electron microscopic study, Mech. Ageing Dev. 2:211–227.

    PubMed  CAS  Google Scholar 

  • Sri-Skanda-Rajah-Sivayoham, I., and Ratnaike, V. T., 1975, Rothmund-Thomson syndrome in an Oriental patient, Ann. Ophthalmol. 7:417–420.

    PubMed  CAS  Google Scholar 

  • Srivastava, R. N., Gupta, P. C., Mayekar, G., and Roy, S., 1974, Cockayne’s syndrome in two sisters, Acta Paediatr. Scand. 63:461–464.

    PubMed  CAS  Google Scholar 

  • Stearns, E. L., MacDonnell, J. A., Kaufman, B. J., Padua, R., Lucman, T. S., Winter, J. S. D., and Faiman, C., 1974, Declining testicular function with age, Am. J. Med. 57:761–766.

    PubMed  CAS  Google Scholar 

  • Steele, R. W., and Bass, J. W., 1970, Hallermann-Streiff syndrome: Clinical and prognostic considerations, Am. J. Dis. Child. 120:462–465.

    PubMed  CAS  Google Scholar 

  • Stein, G. S., and Stein, J. L., 1976, In vitro studies of transcription as a function of age in mammalian cells, Interdiscip. Top. Gerontol. 10:83–99.

    CAS  Google Scholar 

  • Strober, W., Wochner, R. D., Barlow, M. H., McFarlin, D. E., and Waldmann, T. A., 1968, Immunoglobulin metabolism in ataxia telangiectasia, J. Clin. Invest. 47:1905–1915.

    PubMed  CAS  Google Scholar 

  • Tadjoedin, M. K., and Fraser, F. C., 1965, Heredity of ataxia telangiectasia (Louis-Bar syndrome), Am. J. Dis. Child. 110:64–68.

    PubMed  CAS  Google Scholar 

  • Talbot, N. B., Butler, A. M., Pratt, E. L., MacLachlan, E. A., and Tannheimer, J., 1945, Progeria: Clinical, metabolic and pathologic studies on a patient, Am. J. Dis. Child. 69:267–279.

    Google Scholar 

  • Tanenbaum, M. H., 1965, Werner’s syndrome: Progeria of the adult, Arch. Intern. Med. 116:499–504.

    PubMed  CAS  Google Scholar 

  • Tao, L. C., Stecker, E., and Gardner, H. A., 1971, Werner’s syndrome and acute myeloid leukemia, Can. Med. Assoc. J. 105:951–953.

    PubMed  Google Scholar 

  • Tattersall, R. B., and Fajans, S. S., 1975, A difference between the inheritance of classical juvenile-onset and maturity-onset type of diabetes of young people, Diabetes 24:44–53.

    PubMed  CAS  Google Scholar 

  • Taylor, A. M. R., Harnden, D. G., Arlett, C. F., Harcourt, S. A., Lehmann, A. R., Stevens, S., and Bridges, B. A., 1975, Ataxia telangiectasia: A human mutation with abnormal radiation sensitivity, Nature (London) 258:427–429.

    CAS  Google Scholar 

  • Taylor, W. B., 1957, Rothmund’s syndrome—Thomson’s syndrome, Arch. Dermatol. 75:236–244.

    CAS  Google Scholar 

  • Taymor, M. L., Toshihiro, A., and Pheteplace, C., 1968, Serum levels of FSH and LH by radioimmunoassay, in: Gonadotropins 1968, Proceedings of the Workshop Conference—Vista Hermosa, More., Mexico (Rosemberg, ed.), pp. 349–365, Geron-X, California.

    Google Scholar 

  • Thannhauser, S. J., 1945, Werner’s syndrome (progeria of the adult) and Rothmund’s syndrome: Two types of closely related heredofamilial atrophic dermatosis with juvenile cataracts and endocrine features: A critical study with five new cases, Ann. Intern. Med. 23:559.

    Google Scholar 

  • Thomsen, M., Platz, P., Ortved Andersen, O., Christy, M., Lyngsoe, J., Nerup, J., Rasmussen, K., Ryder, L. P., Staub Nelsen, L., and Svejgaard, A., 1975, MLC typing in juvenile diabetes mellitus and idiopathic Addison’s disease, Transplant. Rev. 22:125–147.

    PubMed  CAS  Google Scholar 

  • Thomson, M. S., 1936, Poikiloderma congénitale, Br. J. Dermatol. 48: 221–234.

    Google Scholar 

  • Tibbetts, P. G., Rose, H. D., and Kersting, D. W., 1968, Werner’s syndrome, Wis. Med. J. 67: 550–557.

    PubMed  CAS  Google Scholar 

  • Tokunaga, M., Futami, T., Wakamatsu, E., Endo, M., and Yosizawa, Z., 1975, Werner’s syndrome as “hyaluronuria,” Clin. Chim. Acta 62:89–96.

    PubMed  CAS  Google Scholar 

  • Turner, H. H., 1938, A syndrome of infantilism, congenital webbed neck and cubitus valgus, Endocrinology 23:566–574.

    Google Scholar 

  • Ufermann, K., Heege-Dohr, R., and Kosenow, W., 1973, Ocular manifestation in Cockayne’s syndrome, Klin. Monatsbl. Augenheilkd. 162:655–658.

    PubMed  CAS  Google Scholar 

  • Ungar, B., Stocks, A. E., Martin, F. I. R., Whittingham, S., and Mackay, I. R., 1968, Intrinsic factor antibody, parietal-cell antibody, and latent pernicious anemia in diabetes mellitus, Lancet 2:415–418.

    PubMed  CAS  Google Scholar 

  • Unger, R. H., 1976, Diabetes and the alpha cell, Diabetes 25:136–151.

    PubMed  CAS  Google Scholar 

  • Valdiserri, L., and Stricchiola, G., 1974, Hutchinson-Gilford progeria in a 14-year-old adolescent, Chir. Organi Mov. 61:291–300.

    PubMed  CAS  Google Scholar 

  • Van Campenhout, J., Antaki, A., and Rasio, E., 1973, Diabetes mellitus and thyroid autoimmunity in gonadal dysgenesis, Fertil. Steril. 24:1–9.

    PubMed  Google Scholar 

  • Vandaele, R., 1973, Werner’s syndrome: Familial ulcerous scleroderma with cataract and diabetes, Arch. Belg. Dermatol. Syphiligr. 29:251–254.

    PubMed  CAS  Google Scholar 

  • Viegas, J., Souza, P. L., and Salzano, F. M., 1974, Progeria in twins, J. Med. Genet. 11:384–386.

    PubMed  CAS  Google Scholar 

  • Villee, D. B., Nichols, G., Jr., and Talbot, N. B., 1969, Metabolic studies in two boys with classical progeria, Pediatrics 43: 207–216.

    PubMed  CAS  Google Scholar 

  • Vincent, R. A., Sheridan, R. B., and Huang, P. C., 1975, DNA strand breakage repair in ataxia telangiectasia fibroblast-like cells, Mutat. Res. 33:357–366.

    PubMed  Google Scholar 

  • Vracko, R., and Benditt, E. P., 1974, Manifestations of diabetes mellitus: Their possible relationships to an underlying cell defect, Am. J. Pathol. 75:204–223.

    PubMed  CAS  Google Scholar 

  • Vracko, R., and Benditt, E. P., 1975, Restricted replicative life-span of diabetic fibroblasts in vitro: Its relation to microangiopathy, Fed. Proc. Fed. Am. Soc. Exp. Biol. 34:68–70.

    CAS  Google Scholar 

  • Wahl, J. W., and Ellis, P. P., 1965, Rothmund-Thomson syndrome, Am. J. Ophthalmol. 60: 722–726.

    PubMed  CAS  Google Scholar 

  • Walburg, H. E., 1975, Radiation-induced life shortening and premature aging, Adv. Radiat. Biol. 5:145–179.

    Google Scholar 

  • Waldmann, T. A., and McIntire, K. R., 1972, Serum-alpha-fetoprotein levels in patients with ataxia-telangiectasia, Lancet 2:1112–1115.

    PubMed  CAS  Google Scholar 

  • Wells, R. S., 1972, Werner’s syndrome: Acrogeria, Proc. R. Soc. Med. 65:525–526.

    PubMed  CAS  Google Scholar 

  • Welsh, O., 1975, Study of a family with a new progeroid syndrome, Birth Defects: Orig. Artie. Ser. 11:25–38.

    CAS  Google Scholar 

  • Werder, E. A., Murset, G., Illig, R., and Prader, A., 1975, Hypogonadism and parathyroid adenoma in congenital poikiloderma (Rothmund-Thomson syndrome), Clin. Endocrinol. (Oxford) 4: 75–82.

    CAS  Google Scholar 

  • Werner, O., 1904, Über Katarakt in Verbindung mit Sklerodermie (doctoral dissertation, Kiel University), Schmidt and Klaunig, Kiel, Germany.

    Google Scholar 

  • Wertelecki, W., Fraumeni, J. F., and Mulvihill, J. J., 1970, Non-gonadal neoplasia in Turner’s syndrome, Cancer 26:485–488.

    PubMed  CAS  Google Scholar 

  • Wicks, A. C., and Wall, D. W., 1974, Werner’s syndrome: A case report in a Rhodesian African, Cent. Afr. J. Med. 20:251–254.

    PubMed  CAS  Google Scholar 

  • Wiedemann, H. R., 1969, Some progeroid cases and their diagnostic classification, Z. Kinderheilkd. 107:91–106.

    PubMed  CAS  Google Scholar 

  • Yasuhara, M., Kiyokane, K., Sakai, T., Oiwa, T., and Hashi, N., 1974, A case of Werner’s syndrome, Jpn. J. Hum. Genet. 19:86–87.

    CAS  Google Scholar 

  • Zacharski, L. R., and McIntyre, O. R., 1973, Tissue factor (thromboplastin, Factor III) synthesis by cultured cells, J. Med. 4:118–131.

    CAS  Google Scholar 

  • Zackai, A. H., Weber, D., and Noth, R., 1974, Cardiac findings in Werner’s syndrome, Geriatrics 29:141–148.

    PubMed  CAS  Google Scholar 

  • Zamith, V. A., Campos, J. V., and Chizzotti, M. T., 1974, Rothmund’s syndrome: Serum and urine aminogram—Study of a family, Rev. Bras. Pesqui. Med. Biol. 7:23–27.

    PubMed  CAS  Google Scholar 

  • Zeldis, S. M., Nemerson, Y., Pitlick, F. A., and Lentz, T. L., 1972, Tissue factor (thromboplastin): Localization to plasma membranes by peroxidase-conjugated antibodies, Science 175: 766–768.

    PubMed  CAS  Google Scholar 

  • Zonana, J., and Rimoin, D. L., 1976, Current concepts in genetics: Inheritance of diabetes mellitus, N. Engl. J. Med. 295:603–605.

    PubMed  CAS  Google Scholar 

  • Zucker-Franklin, D., Rifkin, H., and Jacobson, H. G., 1968, Werner’s syndrome: An analysis of ten cases, Geriatrics 23:123–135.

    PubMed  CAS  Google Scholar 

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Goldstein, S. (1978). Human Genetic Disorders That Feature Premature Onset and Accelerated Progression of Biological Aging. In: Schneider, E.L. (eds) The Genetics of Aging. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-2445-4_8

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