CHRNA7 triplication associated with cognitive impairment and neuropsychiatric phenotypes in a three-generation pedigree-Reference-Cited by-同舟云学术

CHRNA7 triplication associated with cognitive impairment and neuropsychiatric phenotypes in a three-generation pedigree

Published:2014-01-15 Issue:9 Volume:22 Page:1071-1076
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Soler-Alfonso Claudia,Carvalho Claudia MB,Ge Jun,Roney Erin K,Bader Patricia I,Kolodziejska Katarzyna E,Miller Rachel M,Lupski James R,Stankiewicz Pawel,Cheung Sau Wai,Bi Weimin,Schaaf Christian P

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2013302.pdf

Reference32 articles.

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3. Shinawi M, Schaaf CP, Bhatt SS et al: A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes. Nat Genet 2009; 41: 1269–1271.

4. Cooper GM, Coe BP, Girirajan S et al: A copy number variation morbidity map of developmental delay. Nat Genet 2011; 43: 838–846.

5. Sahoo T, Theisen A, Rosenfeld JA et al: Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems. Genet Med 2011; 13: 868–880.

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