Recurrent Chromosome 16p13.1 Duplications Are a Risk Factor for Aortic Dissections-Reference-Cited by-同舟云学术

Recurrent Chromosome 16p13.1 Duplications Are a Risk Factor for Aortic Dissections

Published:2011-06-16 Issue:6 Volume:7 Page:e1002118
ISSN:1553-7404
Container-title:PLoS Genetics
language:en
Short-container-title:PLoS Genet

Author:

Kuang Shao-Qing,Guo Dong-Chuan,Prakash Siddharth K.,McDonald Merry-Lynn N.,Johnson Ralph J.,Wang Min,Regalado Ellen S.,Russell Ludivine,Cao Jiu-Mei,Kwartler Callie,Fraivillig Kurt,Coselli Joseph S.,Safi Hazim J.,Estrera Anthony L.,Leal Suzanne M.,LeMaire Scott A.,Belmont John W.,Milewicz Dianna M.,

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics(clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Reference32 articles.

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3. How segmental duplications shape our genome: recent evolution of ABCC6 and PKD1 Mendelian disease genes.;O Symmons;Mol Biol Evol,2008

4. Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.;FD Hannes;J Med Genet,2009

5. Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.;R Ullmann;Hum Mutat,2007

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