Literature DB >> 6644765

C heterochromatin variation in couples with recurrent early abortions.

A Maes, C Staessen, L Hens, E Vamos, M Kirsch-Volders, M C Lauwers, E Defrise-Gussenhoven, C Susanne.   

Abstract

The possible influence of the high polymorphic C heterochromatic regions of human chromosomes 1, 9, 16, and Y on meiotic chromosome segregation was investigated. Faulty chromosome segregation may be the result of either an abnormal quantity of C heterochromatin on the homologues, or disequilibrium between the homologues. The aim of our study was to determine whether either a variation in the amounts of total C heterochromatin or differences in the amounts of C heterochromatin between homologues could lead to faulty chromosome segregation. The study was performed on C banded metaphases obtained from peripheral lymphocyte cultures of 15 couples with recurrent early abortions and 15 control couples, all Caucasians. Analysis of variance was first performed on separate metaphases to measure intra-individual, inter-individual, and between population variation in a hierarchical model. Since the significant intra-individual differences covered the other parameters we performed, secondly, a one way analysis of variance on the mean values of metaphases per person in order to measure the inter-individual and between population variation. The results did not show a relationship between C heterochromatin lengths and occurrence of recurrent abortions.

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Year:  1983        PMID: 6644765      PMCID: PMC1049148          DOI: 10.1136/jmg.20.5.350

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  28 in total

1.  Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families.

Authors:  J Boué; J L Taillemite; P Hazael-Massieux; C Léonard; A Boué
Journal:  Humangenetik       Date:  1975-09-20

2.  Attraction between centric heterochromatin of human chromosomes.

Authors:  M Schmid; W Vogel; W Krone
Journal:  Cytogenet Cell Genet       Date:  1975

3.  Chromosome polymorphism in a human newborn population. II. Potentials of polymorphic chromosome variants for characterizing the idiogram of an individual.

Authors:  H Müller; H P Klinger; M Glasser
Journal:  Cytogenet Cell Genet       Date:  1975

4.  Human Q and C chromosomal variations: distribution and incidence.

Authors:  W H McKenzie; H A Lubs
Journal:  Cytogenet Cell Genet       Date:  1975

5.  Morphologic variability of human chromosomes: polymorphism of constitutive heterochromatin.

Authors:  P K Ghosh; I P Singh
Journal:  Hum Genet       Date:  1976-05-19       Impact factor: 4.132

6.  A simple technique for demonstrating centromeric heterochromatin.

Authors:  A T Sumner
Journal:  Exp Cell Res       Date:  1972-11       Impact factor: 3.905

7.  Marker chromosomes in parents of spontaneous abortuses.

Authors:  S Holbek; U Friedrich; J G Lauritsen; J Therkelsen
Journal:  Humangenetik       Date:  1974

8.  Myths and mechanisms of meiosis.

Authors:  B John
Journal:  Chromosoma       Date:  1976-03-10       Impact factor: 4.316

9.  The effect of structural aberrations of the chromosomes on reproductive fitness in man. II. Results.

Authors:  P A Jacobs; A Frackiewicz; P Law; C J Hilditch; N E Morton
Journal:  Clin Genet       Date:  1975-09       Impact factor: 4.438

10.  Human chromosomal polymorphism. II. Chromsomal C polymorphism in Mongoloid populations of Central Asia.

Authors:  A I Ibraimov; M M Mirrakhimov; S A Nazarenko; E I Axenrod
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

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  3 in total

1.  C-band length variability and reproductive wastage.

Authors:  M T Rodriguez-Gómez; M J Martín-Sempere; J A Abrisqueta
Journal:  Hum Genet       Date:  1987-01       Impact factor: 4.132

2.  A new variant of chromosome 16.

Authors:  P W Thompson; S H Roberts
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

3.  Heterochromatin and nucleolus organizer regions in cells of patients with malignant and premalignant lymphatic diseases.

Authors:  B Schulze; C Golinski; C Fonatsch
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

  3 in total

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