Trisomy 21 in a child due to paternal nondisjunction as determined by RFA technique. - Suppr | 超能文献

Trisomy 21 in a child due to paternal nondisjunction as determined by RFA technique.

作者信息

Verma R S, Dosik H

出版信息

Jinrui Idengaku Zasshi. 1978 Mar;23(1):17-21. doi: 10.1007/BF01871378.

DOI:10.1007/BF01871378

PMID:78997

Abstract

摘要

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Trisomy 21 in a child due to paternal nondisjunction as determined by RFA technique.

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Double autosomal trisomy and mosaicism for chromosomes no. 8 and no. 21.

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Trisomy-21 in mother and child. Report of a case.母婴21三体综合征。病例报告。

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Unusual chromosome aberrations in 3 children with Down syndrome.3名唐氏综合征患儿的异常染色体畸变

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Parental origin, nondisjunction, and recombination of the extra chromosome 21 in Down syndrome: a study in a sample of the Colombian population.唐氏综合征中21号额外染色体的亲本来源、不分离及重组：对哥伦比亚人群样本的一项研究

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引用本文的文献

1

Human chromosomal heteromorphisms in American blacks. III. Evidence for racial differences in RFA color and QFQ intensity heteromorphisms.美国黑人的人类染色体异态性。III. RFA颜色和QFQ强度异态性种族差异的证据。

Hum Genet. 1981;56(3):329-37. doi: 10.1007/BF00274688.

2

A possible cause of non-disjunction of additional chromosome 21 in Down syndrome.唐氏综合征中额外的21号染色体不分离的一个可能原因。

Mol Gen Genet. 1986 Mar;202(3):339-41. doi: 10.1007/BF00333259.