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O. Podugolnikova, I. Parfenova, H. Sushanlo, A. Prokofieva-Belgovskaja (1979)
The quantitative analysis of polymorphism on human chromosomes 1, 9, 16, and YHuman Genetics, 49
(1977)
Le r d e des anomalies chromosomiques dans les khecs de la reproduction
(1977)
Le r d e des anomalies chromosomiques dans
(1970)
Etude de l ' aneuploidie observee dans les cultures de sang et de moelle en fonction du nombre et de la longeur des chromosomes de chaque groupe et de I ' bge et du sexe des sujets
A. Sumner (1972)
A simple technique for demonstrating centromeric heterochromatin.Experimental cell research, 75 1
P. Moorhead, P. Nowell, W. Mellman, D. Battips, D. Hungerford (1960)
Chromosome preparations of leukocytes cultured from human peripheral blood.Experimental cell research, 20
(1960)
Chromosome preparations of leucocytes cultures from human periopheral blood
C. Boudéne (1984)
Mutagenicity, carcinogenicity and teratogenicity of industrial pollutants
J. Azumi, Y. Nakagome, E. Matsunaga (1979)
A new approach in the evaluation of C-positive variants in manJapanese Journal of Human Genetics, 24
S. Galloway, K. Buckton (1978)
Aneuploidy and ageing: chromosome studies on a random sample of the population using G-banding.Cytogenetics and cell genetics, 20 1-6
(1972)
A simple technique for
JacquelineA. Robinson (1973)
Origin of extra chromosome in trisomy 21.Lancet, 1 7795
Xue-Wen Wang (1967)
Standardization in human cytogenetics.British Medical Journal, 4
(1981)
Detecting inherent parental tendency to non-disjunction
Erdtmann (1982)
Aspects of Evaluation, significance and evolution of human c-band heteromorphismHum. Genet., 61
J. Ford, P. Lester (1978)
Chromosomal variants and nondisjunction.Cytogenetics and cell genetics, 21 5
M. Kirsch‐Volders, M. Radman, P. Jeggo, L. Verschaeve (1984)
Molecular Mechanisms of Mutagenesis and Carcinogenesis
M. Kirsch‐Volders, L. Hens, H. Berghe, B. Scholberg, C. Susanne (1982)
Chromosome distribution studies in XXY karyotypes.Journal of Medical Genetics, 19
The aneuploidy frequencies have been stuided in vitro in lymphocytes from couples with recurent abortions, from parents of a trisomic child and from control couples with at least two normal children; c-heterochromatin variants have been analysed on the same samples by length measurements. A significant increase of hyeperploid cells has been observed in the lymphocytes from parents of a trisomic and couples with recurrent abortions as well. However, no consistent correlation has been found so far between c-heterochromatin varients and an increase of aneuploidy.
Clinical Genetics – Wiley
Published: Sep 1, 1983
Keywords: Aneuploidy; c-heterochromation varients; hyperploidy.
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