Benign copy number changes in clinical cytogenetic diagnostics by array CGH-Reference-Cited by-同舟云学术

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Benign copy number changes in clinical cytogenetic diagnostics by array CGH

Published:2008 Issue:1-4 Volume:123 Page:94-101
ISSN:1424-8581
Container-title:Cytogenetic and Genome Research
language:en
Short-container-title:Cytogenet Genome Res

Author:

Whitby H.,Tsalenko A.,Aston E.,Tsang P.,Mitchell S.,Bayrak-Toydemir P.,Hopkins C.,Peters G.,Bailey D.K.,Bruhn L.,Brothman A.R.

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics,Molecular Biology

Cited by 9 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. Copy number variation of the REXO1L1 gene cluster; euchromatic deletion variant or susceptibility factor?;European Journal of Human Genetics;2016-08-03

2. Expansion of a 12-kb VNTR containing the REXO1L1 gene cluster underlies the microscopically visible euchromatic variant of 8q21.2;European Journal of Human Genetics;2013-09-18

3. A Novel Pseudo-Dicentric Variant of 16p11.2q11.2 Contains Euchromatin from 16p11.2p11.1 and Resembles Pathogenic Duplications of Proximal 16q;Cytogenetic and Genome Research;2013

4. Another Family with a Euchromatic Duplication Variant of 9q13-q21.1 Derived from Segmentally Duplicated Pericentromeric Euchromatin;Cytogenetic and Genome Research;2013

5. 16p11.2–p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2;European Journal of Human Genetics;2012-07-25

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