Reevaluation of the origin of a marker chromosome in a patient with 47,XX,r(13)(p11q34), +mar by molecular cytogenetics-Reference-Cited by-同舟云学术

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Reevaluation of the origin of a marker chromosome in a patient with 47,XX,r(13)(p11q34), +mar by molecular cytogenetics

Published:2008-06-28 Issue:6 Volume:42 Page:323-325
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Cooper L. F.,Coss C. A.,Jabs E. W.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1992.tb03266.x/fullpdf

Reference7 articles.

1. Two subsets of alphoid repetitive DNA show preferential localization in the pericentric regions of chromosomes 13, 18, 21;Devilee;Cytogenet Cell Genet,1986

2. Organization of a repetitive human 1.8 kb Kpnl sequence localized in the heterochromatin of chromosome 15;Higgins;Chromosoma:,1985

3. Two different structural abnormalities of chromosome 13 in offspring of chromosomally normal parents with two fragile sites;Mules;Clin Genet,1983

Cited by 3 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. Live‐born autosomal ring chromosomes at the Johns Hopkins Hospital Cytogenomics Laboratory: Case series—Spanning 52 years of experience in a single center;American Journal of Medical Genetics Part A;2023-10-09

2. FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15: II. Review of the literature;American Journal of Medical Genetics;1998-02-03

3. Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group children;American Journal of Medical Genetics;1995-03-13

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