Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family-Reference-Cited by-同舟云学术

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Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family

Published:2010-12-28 Issue:2 Volume:156 Page:225-232
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Shen Yiping,Chen Xiaoli,Wang Liwen,Guo Jin,Shen Jianliang,An Yu,Zhu Haitao,Zhu Yanli,Xin Ruolei,Bao Yihua,Gusella James F.,Zhang Ting,Wu Bai-Lin

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics(clinical)

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.b.31147/fullpdf

Reference21 articles.

1. Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals;Bijlsma;Eur J Med Genet,2009

2. Large, rare chromosomal deletions associated with severe early-onset obesity;Bochukova;Nature,2010

3. The association analysis of TBX6 polymorphism with susceptibility to congenital scoliosis in a Chinese Han population;Fei;Spine (Phila., PA 1976),2010

4. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder;Fernandez;J Med Genet,2010

5. A novel microdeletion at 16p11.2 harbors candidate genes for aortic valve development, seizure disorder, and mild mental retardation;Ghebranious;Am J Med Genet Part A,2007

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