Clinical relevance of small copy-number variants in chromosomal microarray clinical testing-Reference-Cited by-同舟云学术

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Clinical relevance of small copy-number variants in chromosomal microarray clinical testing

Published:2017-04 Issue:4 Volume:19 Page:377-385
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Hollenbeck Dana,Williams Crescenda L.,Drazba Kathryn,Descartes Maria,Korf Bruce R.,Rutledge S. Lane,Lose Edward J.,Robin Nathaniel H.,Carroll Andrew J.,Mikhail Fady M.

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/gim2016132.pdf

Reference40 articles.

Cited by 24 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. DLG2 intragenic exonic deletions reinforce the link to neurodevelopmental disorders and suggest a potential association with congenital anomalies and dysmorphism;Genetics in Medicine;2024-01

2. Systematic analysis of copy number variants of uncertain significance partially overlapping with the haploinsufficient or triplosensitive genes in clinical testing;Annals of Medicine;2023-11-02

3. Homozygous 22q11.2 distal type II microdeletion is associated with syndromic neurodevelopmental delay;American Journal of Medical Genetics Part A;2023-06-27

4. Systematic assessment of the contribution of structural variants to inherited retinal diseases;Human Molecular Genetics;2023-02-22

5. Systematic assessment of the contribution of structural variants to inherited retinal diseases;2023-01-03

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