Skip to main content

Aspects of evaluation, significance, and evolution of human C-band heteromorphism

Summary

The C-band heteromorphism may be evaluated in different forms. The results obtained from classification are easily influenced by subjective factors, and the conclusions of such types of data are acceptable only if they are well matched with a control. The length measurements is simple to obtain, and a quantitative presentation of the data, with correction for the contraction stage of the chromosomes, is considered the most effecient method to evaluate the C-band size heteromorphism. Excluding the acrocentrics, whose short arms present a complex heteromorphism, and the chromosome Y, whose variable C band is terminal, all others present C-band location heteromorphism except pair 16. It is possible to multiply the detectable heteromorphisms in some bands by using diverse staining methods. The present state of knowledge about the role of heterochromatin in the cell is analyzed, as is the effect of C-band variability on the phenotype, the reproductive fitness, and the individual viability. Although a great amount of data is available, no result can be considered definitive as yet. Aspects in which the use of C-band heteromorphisms are profitable are considered.

This is a preview of subscription content, access via your institution.

References

  • Abe T, Morita M, Kawai K (1975) Cd banding of human chromosomes observed in the C-banding procedure. Lancet II:981

    Google Scholar 

  • Angell RR, Jacobs RA (1975) Lateral asymmetry in human constitutive heterochromatin. Chromosoma 51:301–310

    Google Scholar 

  • Angell RR, Jacobs PA (1978) Lateral asymmetry in human constitutive heterochromatin: Frequency and inheritance. Am J Hum Genet 30: 144–152

    Google Scholar 

  • Arrighi FE, Hsu TC (1971) Localization of heterochromatin in human chromosomes. Cytogenet Cell Genet 10:81–86

    Google Scholar 

  • Atkin NB (1977) Chromosome 1 heteromorphism in patients with malignant disease: A constitutional marker for a high-risk group? Br Med J 1:358

    Google Scholar 

  • Atkin NB, Baker MC (1977) Pericentric inversion of chromosome 1: Frequency and possible association with cancer. Cytogenet Cell Genet 19:180–184

    Google Scholar 

  • Atkin NB, Pickthall VJ (1977) Chromosome 1 in 14 ovarian cancers: Heterochromatin variants and structural changes. Hum Genet 38: 25–33

    Google Scholar 

  • Azumi J, Nakagome Y, Matsunaga E (1979) A new approach in the evaluation of C-positive variants in man. Jpn J Hum Genet 24: 99–104

    Google Scholar 

  • Azumi J, Nakagome Y, Oka S, Matsunaga E (1980) A new approach in the evaluation of the chromosome variants in man. II. Paris without Q or C (qh) variants. Hum Genet 55:75–79

    Google Scholar 

  • Balíček P, Žižka J, Sakalská H (1977) Length of human constitutive heterochromatin in relation to chromosome contraction. Hum Genet 38:189–193

    Google Scholar 

  • Balíček P, Žižka J, Skalská H (1978) Variability and familial transmission of constitutive heterochromatin of human chromosomes evaluated by the method of linear measurement. Hum Genet 42: 257–265

    Google Scholar 

  • Beltran IC, Robertson FW, Page BM (1979) Human Y chromosome variation in normal and abnormal babies and their fathers. Ann Hum Genet 42:315–325

    Google Scholar 

  • Berger R, Bernheim A, Coniat M, Vecchione D (1979) C-banding studies in various blood disorders. Cancer Genet Cytogenet 1:95–102

    Google Scholar 

  • Bobrow M, Pearson PL, Collacott HEAC (1971) Para-nucoleolar position of the human Y chromosome in the interphase nuclei. Nature 232:556–557

    Google Scholar 

  • Boué J, Taillmite JL, Hazael-Massieux P, Léonard C, Boué A (1975) Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families. Humangenetik 30:217–224

    Google Scholar 

  • Brito-Babapulle V (1981) Lateral asymmetry in human chromosome 1, 2, 4, 15 and 16. Cytogenet Cell Genet 29:198–202

    Google Scholar 

  • Brøgger A, Urdal T, Larse FB, Lavik NJ (1977) No evidence for a correlation between behavior and the size of the Y chromosome. Clin Genet 11:349–358

    Google Scholar 

  • Brown T, Robertson FW, Dawson BM, Hanlin SJ, Page BM (1980) Individual variation of centric heterochromatin in man. Hum Genet 55:367–373

    Google Scholar 

  • Buckton KE, O'Riordan ML, Jacobs PA, Robinson JA, Hill R, Evans HJ (1976) C and Q band polymorphisms in the chromosomes of three human populations. Ann Hum Genet 40:99–111

    Google Scholar 

  • Bühler EM (1980) A synopsis of human Y chromosome. Hum Genet 55:145–175

    Google Scholar 

  • Buys CHCM, Anders GJPA, Gouw WL, Borkent-Ypma JMM, Blenkers-Platter JAM (1979) A comparison of constitutive heterochromatin staining methods in two cases of familial heterochromatin deficiencies. Hum Genet 52:133–138

    Google Scholar 

  • Buys CHCM, Gouw WL, Blenkers JAM, van Dalen CH (1981) Heterogeneity of human chromosome 9 constitutive heterochromatin as revealed by sequential Distamycin A/DAPI staining and C-banding. Hum Genet 57:28–30

    Google Scholar 

  • Carnevale A, Ibanez BB, Castillo V (1976) The segregation of C-band polymorphisms on chromosomes 1, 9, and 16. Am J Hum Genet 28: 412–416

    Google Scholar 

  • Cavalli IJ, Mattevi MS, Erdtmann B, Sbalqueiro IJ, Maia NA (1982) Quantitative analysis of C bands in chromosomes 1, 9, 16 and Y in Caucasian and Japanese males. (In preparation)

  • Chen TR, Kao ML, Marks J, Chen YY (1981) Polymorphic variants in human chromosome 15. Am J Med Genet 9:61–66

    Google Scholar 

  • Craig-Holmes AP, Moore FB, Shaw MW (1975) Polymorphism of human C-band heterochromatin. II. Family studies with suggestive evidence for somatic crossing over. Am J Hum Genet 27:178–189

    Google Scholar 

  • Crossen PE (1975) Variation in the centromeric banding of chromosome 19. Clin Genet 8:218–222

    Google Scholar 

  • Daniel A (1981) Structural differences in pericentric inversions. Application to a model of risk of recombinants. Hum Genet 56:321–328

    Google Scholar 

  • Dar H, Winter ST (1969) A cytogenetic study of familial deafness. J Med Genet 6:298–303

    Google Scholar 

  • De la Chapelle A, Schröder J, Stenstrand K, Fellman J, Herva R, Saarni M, Anttolainen I, Tallila I, Tervalä L, Tallqvist G, Robson EB, Cook PJL, Sanger R (1974) Pericentric inversions of human chromosome 9 and 10. Am J Hum Genet 26:746–766

    Google Scholar 

  • Donlon TA, Magenis RE (1981) Structural organization of the heterochromatic region of human chromosome 9. Chromosoma 84: 353–363

    Google Scholar 

  • Drets ME, Seuánez H (1974) Quantification of heterogeneous human heterochromatin: Microdensitometric analysis of C and G bands. In: Coutinho EM, Fuchs F (eds) Physiology and genetics of reproduction, part A. Plenum Press, New York, pp 29–52

    Google Scholar 

  • Driscoll DJ, Palmer CG, Melman A (1979) Nonhomologous association of C-heterochromatin at human male meiotic prophase. Cytogenet Cell Genet 23:23–32

    Google Scholar 

  • Eiberg H (1974) New selective Giemsa technique for human chromosomes, Cd staining. Nature 248:55

    Google Scholar 

  • Emanuel BS (1978) Compound lateral asymmetry in human chromosome 6: BrdU-dye studies of 6q12→6q14. Am Hum Genet 30: 153–159

    Google Scholar 

  • Erdtmann B, Salzano FM, Mattevi MS, Flores RZ (1981a) Quantitative analysis of C bands in chromosomes 1, 9, and 16 of Brazilian Indians and Caucasoids. Hum Genet 57:58–63

    Google Scholar 

  • Erdtmann B, Salzano FM, Mattevi MS (1981b) Size variability of the Y chromosome distal C-band in Brazilian Indians and Caucasoids. Ann Hum Biol 8:415–424

    Google Scholar 

  • Erdtmann B, Salzano FM, Mattevi MV (1982) Quantitative analysis of C-bands in human chromosomes. Rev Bras Biol (in press)

  • Ferguson-Smith MA (1964) The sites of nucleolus formation in human pachytene chromosomes. Cytogenetics 3:124–134

    Google Scholar 

  • Fitzgerald PH (1973) The nature and inheritance of an elongated secondary constriction of chromosome 9 of man. Cytogenet Cell Genet 12:404–413

    Google Scholar 

  • Ford JH, Lester P (1978) Chromosomal variants and nondisjunction. Cytogenet Cell Genet 21:300–303

    Google Scholar 

  • Fryns JP, Azon M, Jaeken J, Eggermont E, Pedersen JC, Berghe H (1981) Centromeric instability of chromosomes 1, 9, and 16 associated with combined immunodeficiency. Hum Genet 57:108–110

    Google Scholar 

  • Funderburg SJ, Klisak I, Sparkes RS, Westlake J (1980) C-band polymorphism: Comparison between trisomy 21 cases and mentally retarded controls. Am J Med Genet 5:265–269

    Google Scholar 

  • Gagné R, Laberge C, Tanguay R (1973) Aspect cytologique et localisation intranucléaire de l'heterochromatine constitutive des chromosomes C 9 chez l'homme. Chromosoma 41:159–166

    Google Scholar 

  • Gagné R, Luciani JM, Devictor-Vuillet M, Stahl A (1974) C 9 heterochromatin during the first meiotic prophase in human foetal oocyte. Exp Cell Res 85:111–116

    Google Scholar 

  • Galloway SM, Evans HJ (1975) Asymmetrical C-bands and satellite DNA in man. Exp Cell Res 94:454–459

    Google Scholar 

  • Gardner RJM, McGreanor HR, Parslow MI, Vcale AMO (1974) Are 1q+ chromosomes harmless? Clin Genet 6:383–393

    Google Scholar 

  • Geraeds JPM, Pearson PL (1976) Chromosome in human spematozoa. Chromosomes Today 5:23–31

    Google Scholar 

  • Ghosh PK, Rani R, Nand R (1979) Lateral asymmetry of constitutive heterochromatin in human chromosomes. Hum Genet 52:79–84

    Google Scholar 

  • Gosden JR, Spowart G, Lawrie SS (1981) Satellite DNA and cytological staining patterns in heterochromatic inversions of human chromosome 9. Hum Genet 58:276–278

    Google Scholar 

  • Hager HD, Schroeder-Kurth TM, Vogel F (1982) An analysis of nonhomologous chromatid translocations in lymphocyte cultures after Treminon treatment and from patients with Fanconi's anemia and Bloom's syndrome. (In preparation)

  • Halbrecht I, Shabtai F (1976) Human chromosome polymorphism and congenital malformations. Clin Genet 10:113–122

    Google Scholar 

  • Hartung M, Fouet C, Stahl A (1975) L'association au nucléole de l'heterochromatine juxta-centromérique du chromosome 1 de l'homme. Ann Genet (Paris) 18:247–249

    Google Scholar 

  • Hemming L, Burns C (1979) Heterochromatic polymorphism in spontaneous abortions. J Med Genet 16:358–362

    Google Scholar 

  • Holbek S, Friedrich U, Lauritsen JG, Therkelsen AJ (1974) Marker chromosomes in parents of spontaneous abortuses. Humangenetik 25:61–64

    Google Scholar 

  • Howard-Peebles PN (1978) Familial pericentric inversion of chromosome 1 with a note on reproductive risks. Hum Genet 45:123–125

    Google Scholar 

  • Hsu TC (1975) A possible function of constitutive heterochromatin: The bodyguard hypothesis. Genetics (Suppl) 79:137–150

    Google Scholar 

  • Hungerford DA, Ashton FT, Balaban GB, La Badie GU, Messatzzia LR, Haller G, Miller AE (1972) The C-group pachytene bivalent with a locus characteristic for parachromosomally situated particulate bodies (parameres): a provisional map in human males. Proc Natl Acad Sci 69:2165–2168

    Google Scholar 

  • Ibraimov AI, Mirrakhimov MM, Nazarenko SA, Axenrod EI (1982) Human chromosomal polymorphism. II. Chromosomal C polymorphism in Mongoloid populations of central Asia. Hum Genet 60:8–9

    Google Scholar 

  • Jacobs P (1975) The load due to chromosome abnormalities in man. In: Salzano FM (ed) The role of natural selection in human evolution. North-Holland, Amsterdam Oxford, pp 337–352

    Google Scholar 

  • Jacobs PA, Frackiewicz A, Law P, Hilditch CJ, Morton NE (1975) The effect of structural aberrations of the chromosomes on reproductive fitness in man. II. Results. Clin Genet 8:169–178

    Google Scholar 

  • Kaiser P (1980) Pericentrische Inversionen menschlicher Chromosomen. Georg Thieme Verlag, Stuttgart

    Google Scholar 

  • Kim MA (1975) Fluorometrical detection of thymine differences in complementary strands of satellite DNA in human metaphase chromosomes. Humangenetik 28:57–63

    Google Scholar 

  • Kivi S, Mikelsaar AV (1980) Q-and C-band polymorphisms in patients with ovarian or breast carcinoma. Hum Genet 56:111–114

    Google Scholar 

  • Klasen M, Schmid M (1981) An improved method for Y-body identification and confirmation of a high incidence of YY sperm nuclei. Hum Genet 58:156–161

    Google Scholar 

  • Kuhn EM (1978) Mitotic chiasmata and other quadriradials in mitomycin C-treated Bloom's syndrome lymphocytes. Chromosoma 66:287–297

    Google Scholar 

  • Kunze J, Mau G (1975) A 1 and C 9 marker chromosomes in children with combined minor and major malformations. Lancet 1:273

    Google Scholar 

  • Langenbeck U, Hansmann I, Hinney B, Hönig V (1976) On the origin of the supernumerary chromosome in autosomal trisomies with special reference to Down's syndrome. Hum Genet 33:89–102

    Google Scholar 

  • Latt SA, Davidson RL, Lin MS, Gerald PS (1974) Lateral asymmetry in the fluorescence of human Y chromosome stained with 33258 Hoechst. Exp Cell Res 87:427–429

    Google Scholar 

  • Lelikova GP, Benyush VA, Tsvetkova TG (1977) Quantitative analysis of human chromosome polymorphism in near-centromeric heterochromatin (in Russian). Genetika 13:2195–2200

    Google Scholar 

  • Leonard C, Hazael-Massieux P, Bocquet L, Larget-Piet L, Boué J (1975) Inversion péricentrique inv(2)(p11q13) dans de familles non apparentées. Humangenetik 28:121–128

    Google Scholar 

  • Limon J, Gibas Z, Kaluzawski B, Moruzgala T (1979) Demonstration of two different regions of lateral asymmetry in human Y chromosomes. Hum Genet 51:247–252

    Google Scholar 

  • Lin MS, Alfi OS (1978) Variation in lateral asymmetry of human chromosome 1. Cytogenet Cell Genet 21:243–250

    Google Scholar 

  • Lopetegui PH (1980) 1, 9 and 16 C-band heteromorphisms in parents of Down's syndrome patients: Distribution and etiological significance. Jpn J Hum Genet 25:29–37

    Google Scholar 

  • Lubs HA, Patil SA, Kimberling WJ, Brown J, Cohen M, Gerald P, Hecht F, Myrianthopoulos N, Summitt RL (1977) Q and C banding polymorphisms in 7- and 8-year-old children: racial differences and clinical significances. In: Hook EB, Porter IH (eds) Populational cytogenetic studies in humans. Academic Press, New York San Francisco London, pp 133–159

    Google Scholar 

  • Magenis RE, Palmer CG, Wang L, Brown M, Chamberling J, Parks M, Merrit AD, Rivas M, Yu PL (1977) Heredability of chromosome banding variants. In: Hook EB, Porter IH (eds) Population cytogenetic studies in humans. Academic Press, New York San Francisco London, pp 179–188

    Google Scholar 

  • Magenis RE, Donlon TA, Wyandt HE (1978) Giemsa-11 staining of chromosome 1: A newly described heteromorphism. Science 202: 64–65

    Google Scholar 

  • Mason D, Lauder I, Rutovitz D, Spowart G (1975) Measurement of C-bands in human chromosomes. Comput Biol Med 5:179–201

    Google Scholar 

  • Mason DC, Lauder IJ, Spowart G (1978) Automated measurements on human C-bands in family studies. Cytogenet Cell Genet 21:251–266

    Google Scholar 

  • Matsuura J, Mayer M, Jacobs P (1978) A cytogenetic survey of an institution for mentally retarded: II. C-band chromosome heteromorphisms. Hum Genet 45:33–41

    Google Scholar 

  • Mattei MG, Mattei JF, Guichaoua M, Giraud F (1981) Partial inversion of the secondary constriction of chromosome 9. Does it exist? Hum Genet 59:310–316

    Google Scholar 

  • Mikelsaar AV, Ilus T, Kivi S (1978) Variant chromosome 3 (inv 3) in normal newborns and their parents, and in children with mental retardation. Hum Genet 41:109–113

    Google Scholar 

  • Monsalve MV, Erdtmann B, Otto PA, Frotta-Pessoa O (1980) The human Y chromosome: Racial variation and evolution. Rev Bras Genet 3:433–446

    Google Scholar 

  • Muller HJ (1914) A gene for the fourth chromosome of Drosophila. J Exp Zool 17:325–336

    Google Scholar 

  • Müller H, Klinger HP, Glasser M (1975) Chromosome polymorphism in a human newborn population. II. Potential of polymorphic chromosome variants for characterizing the idiogram of an individual. Cytogenet Cell Genet 15:239–255

    Google Scholar 

  • Nielsen J (1978) Large Y chromosome (Yq+) and increased risk of abortion. Clin Genet 13:415–416

    Google Scholar 

  • Nielsen J, Friedrich U, Hreidarsson AB, Zeuthen E (1974) Frequency of 9qh+ and risk of chromosome aberrations in the progeny of individuals with 9qh+. Humangenetik 21:211–216

    Google Scholar 

  • Nielsen J, Hansen KB, Sillensen I, Videbach P (1981) Chromosome abnormalities in newborn children. Physical aspects. Hum Genet 59:194–200

    Google Scholar 

  • Okamoto E, Miller DA, Erlanger BF, Miller OJ (1981) Polymorphism of 5-methylcytosine-rich DNA in human acrocentric chromosomes. Hum Genet 58:255–259

    Google Scholar 

  • Palmer CG, Schroder J (1971) A familial variant of chromosome 9. J Med Genet 8:202–208

    Google Scholar 

  • Pardo D, Luciani JM, Stahl A (1975) Localisation, par hybridation in situ, des gènes de ARN 28S et 18S dans les chromosomes somatiques humaines. Ann Genet (Paris) 18:105–109

    Google Scholar 

  • Paris Conference (1971) Supplement (1975) Standardization in human cytogenetics. Birth Defects XI:9

    Google Scholar 

  • Patil SR, Lubs HA (1974) Spontaneous abortions and long Y chromosomes. Am J Hum Genet 26:66A

    Google Scholar 

  • Patil SR, Lubs HA (1977) A possible association of long Y chromosomes and fetal loss. Hum Genet 35:233–235

    Google Scholar 

  • Pescia G, Gaide AC, Jullard E (1977) Trois familles avec inversion pericentrique du chromosome 9 (inv C9). J Genet Hum 25:121–134

    Google Scholar 

  • Phillips RB (1977) Inheritance of Q and C-band polymorphisms. Can J Genet Cytol 19:405–413

    Google Scholar 

  • Phillips RB (1980) New C band markers of human chromosomes: C band position variants. J Med Genet 17:380–385

    Google Scholar 

  • Podugolnikova OA, Parfenova IV, Sushanlo HM, Prokofieva-Belgovskaja AA (1979a) The quantitative analysis of polymorphism on human chromosomes 1, 9, 16, and Y. I. Description of individual karyotypes. Hum Genet 49:243–250

    Google Scholar 

  • Podugolnikova OA, Sushanlo HM, Parfenova IV, Prokofieva-Belgovskaja AA (1979b) The quantitative analysis of polymorphism on human chromosomes 1, 9, 16, and Y. II. Comparison of the C segments in male and female individuals (group characteristics). Hum Genet 49:251–260

    Google Scholar 

  • Prantera G, Pimpinelli S, Rocchi A (1979) Effects of distamycin A on human leukocytes in vitro. Cytogenet Cell Genet 23:103–107

    Google Scholar 

  • Robinson JA, Buckton KE, Spowart G, Newton M, Jacobs PA, Evans HJ, Hill R (1976) The segregation of human chromosome polymorphisms. Ann Hum Genet 40:113–121

    Google Scholar 

  • Rocchi A, Di Castro M, Prantera G (1979) Effects of DAPI on human leukocytes in vitro. Cytogenet Cell Genet 23:250–254

    Google Scholar 

  • Rotterdam Conference (1974) Second international workshop on human gene mapping. Cytogenet Cell Genet 14:161–480

    Google Scholar 

  • Schaap T, Sagi M, Cohen MM (1980) Chromosome-specific patterns of mitomycin C-induced rearrangements in human lymphocytes. Cytogenet Cell Genet 28:240–250

    Google Scholar 

  • Schmiady H, Sperling K (1976) Length of human C-band in relation to the degree of chromosome condensation. Hum Genet 35:107–111

    Google Scholar 

  • Schmid M, Vogel W, Krone W (1975) Attraction between centric heterochromatin of human chromosomes. Cytogenet Cell Genet 15:66–80

    Google Scholar 

  • Schnedl W (1978) Structure and variability of human chromosomes analyzed by recent techniques. Hum Genet 41:1–9

    Google Scholar 

  • Schweitzer D, Ambros P, Andrle M (1978) Modification of DAPI banding on human chromosomes by prestaining with a DNA binding oligopeptide antibiotic, distamycin A. Exp Cell Res 111:327–332

    Google Scholar 

  • Seabright M, Gregson NM, Johnson M (1980) A lamilial polymorphic variant of chromosome 5. J Med Genet 17:444–446

    Google Scholar 

  • Shabtai F, Halbrecht I (1979) Risk of malignancy and chromosomal polymorphism: A possible mechanism of association. Clin Genet 15:73–77

    Google Scholar 

  • Shabtai F, Weiss S, van der Lijn E, Lewinski U (1978) A new cytogenetic aspect of polycythemia vera. Hum Genet 41:281–287

    Google Scholar 

  • Sigmund J, Schwarz S (1979) Variable substructure in the secondary constriction of the human chromosome 1. Hum Genet 46:1–4

    Google Scholar 

  • Sofuni T, Naruto J, Awa AA (1979) Quantitative analysis of C-bands based on area measurement. Jpn J Hum Genet 24:194–195

    Google Scholar 

  • Soudek D, Sroka H (1978) Inversion of fluorescent segment in chromosome 3: a polymorphic trait. Hum Genet 44:109–115

    Google Scholar 

  • Stahl A, Luciani JM, Devictor M, Capodano AM, Gagné R (1975) Constitutive heterochromatin and micronucleoli in the human oocyte at the diplotene stage. Humangenetik 26:315–327

    Google Scholar 

  • Stahl A, Hartung M, Vagner-Capodano A (1976a) Chromosomal constitution of nucleolus associated chromatin in man. Clin Genet 10:370

    Google Scholar 

  • Stahl A, Hartung M, Vagner-Capodano AM, Fouet C (1976b) Chromosomal constitution of nucleolus-associated chromatin in man. Hum Genet 35:27–34

    Google Scholar 

  • Stallard R, Browner M, Burday MJ (1979) Objective definition of C-band size. Am J Hum Genet 31:111A

    Google Scholar 

  • Stallard R, Haney N, Frank P, Mowrey P, Knops J, Juberg RC (1981) Detecting inherent parental tendency to nondisjunction. Am J Hum Genet 33:123A

    Google Scholar 

  • Steffesen DM, Duffey P, Prensky W (1974) Localization of 5S ribosomal RNA genes on human chromosome 1. Nature 252:741–743

    Google Scholar 

  • Sumner AT (1972) A simple technique for demonstrating centromeric heterochromatin. Exp Cell Res 75:304–306

    Google Scholar 

  • Tharapel AT, Summitt RL (1978) Minor chromosome variation and selected heteromorphisms in 200 unclassifiable mentally retarded patients and 200 normal controls. Hum Genet 41:121–130

    Google Scholar 

  • Tishler PV, Rosner B, Lamborot-Mansur M, Atkins L (1974) Studies on the localization of Y fluorescent body in human interphase nuclei. Humangenetik 22:275–286

    Google Scholar 

  • Tsenghi C, Metaxotou-Stavridaki C, Stratakibenetou M, Kalpini-Mavrou A, Matsaniotis N (1976) Chromosome studies in couples with repeated spontaneous abortions. Obstet Gynecol 47:463–468

    Google Scholar 

  • Tsvetkova TG (1979) Chromosome polymorphism and reproductive dysfunction in man. III. Extreme C-variants of autosomes: analysis of distribution and combination in the karyotype (in Russian). Genetika 16:2210–2216

    Google Scholar 

  • Tsvetkova TG, Yankova MF (1979) Human chromosome polymorphism and reproductive failure. II. C-variants (in Russian). Genetika 15:1870–1879

    Google Scholar 

  • Van Dyke DL, Palmer CG, Nance WE, Yu PL (1977) Chromosome polymorphism and twin zygosity. Am J Hum Genet 29:431–447

    Google Scholar 

  • Verma RS, Lubs HA (1975) Variation in human acrocentric chromosomes with acridine orange reverse banding. Humangenetik 30: 225–235

    Google Scholar 

  • Verma RS, Dosik, Lubs HA (1978) Size and pericentric inversion heteromorphisms of secondary constriction regions (h) of chromosomes 1, 9, and 16 as detected by CBG technique in Caucasians: Classification, frequencies and incidence. Am J Med Genet 2:331–339

    Google Scholar 

  • Verma RS, Rodrigues J, Dosik H (1981) Human chromosome heteromorphism in American Blacks: II. Higher incidence of pericentric inversions of secondary constriction regions (h). Am J Med Genet 8:17–25

    Google Scholar 

  • Viégas J, Salzano FM (1978) C-bands in chromosomes 1, 9, and 16 of twins. Hum Genet 45:127–130

    Google Scholar 

  • Vogel F, Schroeder TM (1974) The internal order of the interphase nucleus. Humangenetik 25:265–297

    Google Scholar 

  • Wachtler F, Musil R (1980) On the structure and polymorphism of the human chromosomeno. 15. Hum Genet 56:115–118

    Google Scholar 

  • Wang HS, Hamerton JL (1979) C-band polymorphisms of chromosomes 1, 9, and 16 in four subgroups of mentally retarded patients and a normal control population. Hum Genet 51:269–275

    Google Scholar 

  • Ward BE, Henry GP, Robinson A (1980) Cytogenetic studies in 100 couples with recurrent spontaneous abortions. Am J Hum Genet 32:549–554

    Google Scholar 

  • Wegner H, Pawlowitzki IH (1981) Quantification of C-band polymorphism by centromeric elevations (Ce-bands). Hum Genet 58: 302–305

    Google Scholar 

  • Wyandt HE, Iorio RJ (1973) Human Y-chromatin. III. The nucleolus. Exp Cell Res 81:468–473

    Google Scholar 

Download references

Author information

Affiliations

Authors

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Erdtmann, B. Aspects of evaluation, significance, and evolution of human C-band heteromorphism. Hum Genet 61, 281–294 (1982). https://doi.org/10.1007/BF00276592

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00276592

Keywords

  • Internal Medicine
  • Metabolic Disease
  • Present State
  • Length Measurement
  • Staining Method