A Marfan syndrome-like phenotype caused by a neocentromeric supernumerary ring chromosome 15-Reference-Cited by-同舟云学术

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A Marfan syndrome-like phenotype caused by a neocentromeric supernumerary ring chromosome 15

Published:2016-10-14 Issue:1 Volume:173 Page:268-273
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Quinonez Shane C.¹²,Gelehrter Thomas D.²³,Uhlmann Wendy R.²³

Affiliation:

1. Department of Pediatrics and Communicable Diseases; University of Michigan Medical School; Ann Arbor Michigan

2. Department of Internal Medicine; University of Michigan; Ann Arbor Michigan

3. Department of Human Genetics; University of Michigan; Ann Arbor Michigan

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.38000/fullpdf

Reference41 articles.

1. Mosaic monosomy of a neocentric ring chromosome maps brachyphalangy and growth hormone deficiency to 13q31. 1-13q32.3;Amor;Am J Med Genet Part A,2005

2. Formation of a minichromosome by excision of the proximal region of 17q in a patient with von Recklinghausen neurofibromatosis;Andersen;Cytogenet Cell Genet,1990

3. Mechanisms and consequences of small supernumerary marker chromosomes: From barbara McClintock to modern genetic-counseling issues;Baldwin;Am J Hum Genet,2008

4. Burnside RD Ibrahim J Flora C Schwartz S Tepperberg JH Papenhausen PR 2009

5. Interstitial deletion 11(p11.12p11.2) and analphoid marker formation results in inherited Potocki-Shaffer syndrome;Chuang;Am J Med Genet Part A,2005

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. Molecular cytogenetic characterization of small supernumerary marker 15 in infertile male: A case report;Experimental and Therapeutic Medicine;2020-02-21

2. Ring chromosome 15 – cytogenetics and mapping arrays: a case report and review of the literature;Journal of Medical Case Reports;2018-11-16

3. Intragenic multi-exon deletion in the FBN1 gene in a child with mildly dilated aortic sinus: a retrotransposal event;Journal of Human Genetics;2017-03-23

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