The application of DNA recombinant technology to the analysis of the human genome and genetic disease Kay E. Davies Review Articles 01 October 1981 Pages: 351 - 357
Assignment of the glyoxalase II gene (HAGH) to human chromosome 16 Neville K. HoneyThomas B. Shows Original Investigations 01 October 1981 Pages: 358 - 361
Cytogenetic investigation of six patients with X isochromosomes, i(Xq), and of two subjects with isodicentric X chromosomes, idic(Xq) M. GaálJ. LászlóP. Bösze Original Investigations 01 October 1981 Pages: 362 - 365
Further delineation of X-linked mental retardation D. S. HerbstH. G. DunnL. W. Krywaniuk Original Investigations 01 October 1981 Pages: 366 - 372
Clinical and endocrine spectrum in patients with the 45,X/46,XY karyotype Susana KofmanGregorio Pérez-PalaciosRubén Lisker Original Investigations 01 October 1981 Pages: 373 - 376
Adjacent 2 meiotic disjunction. Report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature David P. DuckettSelwyn H. Roberts Original Investigations 01 October 1981 Pages: 377 - 386
β-Galactosidase-neuraminidase deficiency in adults: Deficiency of a freeze-labile neuraminidase in leukocytes and fibroblasts Yoshiyuki SuzukiHitoshi SakurabaHirokuni Beppu Original Investigations 01 October 1981 Pages: 387 - 389
Etiological study of omphalocele A. CzeizelMárta Vitéz Original Investigations 01 October 1981 Pages: 390 - 395
De novo mutations producing unstable hemoglobins or hemoglobins M G. StamatoyannopoulosP. E. NuteM. Miller Original Investigations 01 October 1981 Pages: 396 - 404
Glucose 6-Phosphate dehydrogenase variants: A unique variant (G6PD Kobe) showed an extremely increased affinity for galactose 6-phosphate and a new variant (G6PD Sapporo) resembling G6PD Pea Ridge H. FujiiS. MiwaT. Sato Original Investigations 01 October 1981 Pages: 405 - 407
Acute leukaemia and the same chromosome abnormality in monozygotic twins S. E. HartleyC. Sainsbury Original Investigations 01 October 1981 Pages: 408 - 410
A new hereditary variant of the PGM1 erythrocyte enzyme system determined by isoelectric focusing V. SachsM. SiemsenBarbara Vollert Original Investigations 01 October 1981 Pages: 411 - 413
Evidence for the derivation of individual hair roots from three progenitor cells Joseph DancisDavid N. SilversMelvin S. Schwartz Original Investigations 01 October 1981 Pages: 414 - 416
A high incidence of mitotic chiasmata in endoreduplicated Bloom's syndrome cells Evelyn Meyer Kuhn Original Investigations 01 October 1981 Pages: 417 - 421
The ataxia telangiectasia clastogenic factor is a low molecular weight peptide Meira ShahamYechiel Becker Original Investigations 01 October 1981 Pages: 422 - 424
The inherited enzymatic defect in porphyria variegata J. Ch. DeybachH. de VerneuilY. Nordmann Original Investigations 01 October 1981 Pages: 425 - 428
Gametic equilibrium of four loci on chromosome 1 Karen Gottlieb Short Communication 01 October 1981 Pages: 429 - 431
Mutagen-induced sister chromatid exchange rate in Bloom syndrome remains unaltered in the presence of Bloom corrective factor Ute Schmidt-PreußPetra MaackHugo W. Rüdiger Short Communications 01 October 1981 Pages: 432 - 433
Glucose-6-phosphate dehydrogenase deficiency in Iraq Hanan A. HamamyThanaa Kh. Saeed Short Communications 01 October 1981 Pages: 434 - 435
Proximal trisomy 13. A family with balanced reciprocal translocation t(8;13) in seven members and Robertsonian translocation t(13;14) in three members S. GilgenkrantzC. DefecheM. J. Gregoire Clinical Case Reports 01 October 1981 Pages: 436 - 440
Congenital osteogenesis imperfecta in three sibs Suzanne BragaE. Passarge Clinical Case Reports 01 October 1981 Pages: 441 - 443
De novo duplication 13q (46,XX,dup(13)(q21→q333)) M. Fraccaro Cases Observed 01 October 1981 Pages: 444 - 444
Three cases of familial pericentric inversion 2 Peter Steinbach Cases Observed 01 October 1981 Pages: 444 - 444
Partial trisomy 13 (q14→qter) due to a familial translocation t(13;18)(q14;q23) Peter Steinbach Cases Observed 01 October 1981 Pages: 444 - 444
Phenotypic manifestation and pericentric inversion 6 Angela Schmidt Cases Observed 01 October 1981 Pages: 445 - 445
Multiple Y-chromosomal aberrations in a patient with mixed gonadal dysgenesis of XO/XY Type Angela SchmidtE. Passarge Cases Observed 01 October 1981 Pages: 445 - 445
Sporadic translocation, inversion, and marker chromosome in prenatal diagnosis Angela SchmidtE. Passarge Cases Observed 01 October 1981 Pages: 445 - 445
Further evidence for the assignment of the steroid sulfatase X-linked ichthyosis locus to the telomer of Xp C. R. MüllerJ. WahlströmDoreen Liebeskind Letter to the Editors 01 October 1981 Pages: 446 - 447
Erratum zu: Zum praktischen Wert des Lymphozytenmodells für die pathogenetische Beurteilung einzelner Serumcholesterinfraktionen des Menschen bei der autosomal-monogenen Hypercholesterinämie Th. WichmannH. -A. FreyeK. Berndt Erratum 01 October 1981 Pages: 448 - 448