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...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
izdano v:Congenit Heart Dis
Main Authors: Goldmuntz, Elizabeth, Paluru, Prasuna, Glessner, Joseph, Hakonarson, Hakon, Biegel, Jaclyn A., White, Peter S., Gai, Xiaowu, Shaikh, Tamim H.
Format: Artigo
Jezik:Inglês
Izdano: 2011
Teme:
Article
Online dostop: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
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki