Microdeletions and Microduplications in Patients with Congenital Heart Disease and Multiple Congenital Anomalies

OBJECTIVE: Multiple genetic syndromes are caused by recurrent chromosomal microdeletions or microduplications. The increasing use of high-resolution microarrays in clinical analysis has allowed the identification of previously undetectable submicroscopic copy number variants (CNVs) associated with g...

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Библиографические подробности
Опубликовано в: :Congenit Heart Dis
Главные авторы: Goldmuntz, Elizabeth, Paluru, Prasuna, Glessner, Joseph, Hakonarson, Hakon, Biegel, Jaclyn A., White, Peter S., Gai, Xiaowu, Shaikh, Tamim H.
Формат: Artigo
Язык:Inglês
Опубликовано: 2011
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Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4575121/
https://ncbi.nlm.nih.gov/pubmed/22010865
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1747-0803.2011.00582.x
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