Abstract
Since the advent of C-banding as a routine diagnostic procedure, the significance of heterochromatic polymorphism has been questioned. Some workers have considered variations in heterochromatin in chromosomes 1 and 9 to be associated with fetal wastage, recurrent abortions, and abnormal phenotypes. Over a 15-month period, this laboratory made a study of the diagnostic significance of heterochromatic variants in 50 couples with a history of recurrent abortions. A control group of 50 couples with at least two normal children and no miscarriages was investigated simultaneously. The results indicated no significant difference in the heterochromatic regions between aborting and non-aborting couples.
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- Boué J., Taillemite J. L., Hazael-Massieux P., Léonard C., Boué A. Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families. Humangenetik. 1975 Sep 20;30(3):217–224. doi: 10.1007/BF00279187. [DOI] [PubMed] [Google Scholar]
- Gardner R. J., McCreanor H. R., Parslow M. I., Veale A. M. Are 1q plus chromosomes harmless? Clin Genet. 1974;6(5):383–393. [PubMed] [Google Scholar]
- Halbrecht I., Shabtay F. Human chromosome polymorphism and congenital malformations. Clin Genet. 1976 Aug;10(2NA-NA-760903-760909):113–122. doi: 10.1111/j.1399-0004.1976.tb00022.x. [DOI] [PubMed] [Google Scholar]
- Kunze J., Mau G. Letter: A1 and C9 marker chromosomes in children with combined minor and major malformations. Lancet. 1975 Feb 1;1(7901):273–273. doi: 10.1016/s0140-6736(75)91167-8. [DOI] [PubMed] [Google Scholar]
- Müller H., Klinger H. P., Glasser M. Chromosome polymorphism in a human newborn population. II. Potentials of polymorphic chromosome variants for characterizing the idiogram of an individual. Cytogenet Cell Genet. 1975;15(4):239–255. doi: 10.1159/000130522. [DOI] [PubMed] [Google Scholar]
- Nielsen J., Friedrich U., Hreidarsson A. B., Zeuthen E. Frequency of 9qh+ and risk of chromosome aberrations in the progeny of individuals with 9qh+. Humangenetik. 1974;21(3):211–216. doi: 10.1007/BF00279014. [DOI] [PubMed] [Google Scholar]
- Scheres J. M. Identification of two Robertsonian translocations with a Giemsa banding technique. Humangenetik. 1972;15(3):253–256. doi: 10.1007/BF00702361. [DOI] [PubMed] [Google Scholar]
- Sumner A. T. A simple technique for demonstrating centromeric heterochromatin. Exp Cell Res. 1972 Nov;75(1):304–306. doi: 10.1016/0014-4827(72)90558-7. [DOI] [PubMed] [Google Scholar]
- Tsenghi C., Metaxotou-Stavridaki C., Strataki-Benetou M., Kalpini-Mavrou A., Matsaniotis N. Chromosome studies in couples with repeated spontaneous abortions. Obstet Gynecol. 1976 Apr;47(4):463–468. [PubMed] [Google Scholar]