Triplication of chromosome Arm 20p due to inherited translocation and secondary nondisjunction-Reference-Cited by-同舟云学术

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Triplication of chromosome Arm 20p due to inherited translocation and secondary nondisjunction

Published:1979 Issue:1 Volume:4 Page:47-50
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Marcus E. S.,Fuller B.,Riccardi V. M.,Lubs Herbert A.

Publisher

Wiley

Subject

Genetics (clinical)

Reference3 articles.

1. : Abnormalities of chromosomes 11 and 20. In (ed): “New Chromosomal Syndromes.” New York: Academic, 1977, pp 245-272.

2. TRISOMY 20 MOSAICISM

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization;American Journal of Medical Genetics Part A;2011-09-21

2. Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U-type exchange model;American Journal of Medical Genetics Part A;2009-03

3. Brachydactyly in a child with duplication-deficiency subsequent to t(15;20)(q25.2;p12.2)mat. Candidate regions on one or both chromosomes?;Clinical Genetics;2008-06-28

4. 20 p duplication as a result of parental translocation: familial case report and a contribution to the clinical delineation of the syndrome;Clinical Genetics;2008-06-28

5. Familial Wolf's syndrome with a hidden 4p deletion by translocation of an 8p segment. Unbalanced inheritance from a maternal translocation (4;8)(p15.3;p22). Case report, review and risk estimates;Clinical Genetics;2008-04-23

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