CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens-Reference-Cited by-同舟云学术

CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens

Published:2016-06 Issue:1 Volume:6 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Wang Binbin,Ji Taoyun,Zhou Xueya,Wang Jing,Wang Xi,Wang Jingmin,Zhu Dingliang,Zhang Xuejun,Sham Pak Chung,Zhang Xuegong,Ma Xu,Jiang Yuwu

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep25954.pdf

Reference104 articles.

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2. Merikangas, A. K., Corvin, A. P. & Gallagher, L. Copy-number variants in neurodevelopmental disorders: promises and challenges. Trends Genet 25, 536–544, 10.1016/j.tig.2009.10.006 (2009).

3. Stankiewicz, P. & Lupski, J. R. Structural variation in the human genome and its role in disease. Annu Rev Med 61, 437–455, 10.1146/annurev-med-100708-204735 (2010).

4. Girirajan, S. et al. Relative burden of large CNVs on a range of neurodevelopmental phenotypes. PLos Genet 7, e1002334, 10.1371/journal.pgen.1002334 (2011).

5. Miller, D. T. et al. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet 86, 749–764, 10.1016/j.ajhg.2010.04.006 (2010).

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