Etiology of nondisjunction in humans-Reference-Cited by-同舟云学术

Etiology of nondisjunction in humans

Published:1995 Issue:S2 Volume:25 Page:38-47
ISSN:0893-6692
Container-title:Environmental and Molecular Mutagenesis
language:en
Short-container-title:Environ. Mol. Mutagen.

Author:

Abruzzo Michael A.,Hassold Terry J.

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Genetics (clinical),Epidemiology

Reference52 articles.

1. (1995): Mechanisms of chromosome nondisjunction in human oocytes. In (ed): “Etiology in Pathogenesis of Down's Syndrome.” New York: Wiley-Liss, Inc., pp 13–26.

2. First meiotic division abnormalities in human oocytes: mechanism of trisomy formation

3. Cytogenetic studies in motile sperm from normal men

4. Chromosome anomalies in human oocytes failing to fertilize after insemination in vitro

5. Methods for studying recombination on chromosomes that undergo nondisjunction

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