Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?-Reference-Cited by-同舟云学术

Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?

Published:2010-05-10 Issue:7 Volume:31 Page:840-850
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Szafranski Przemyslaw,Schaaf Christian P.,Person Richard E.,Gibson Ian B.,Xia Zhilian,Mahadevan Sangeetha,Wiszniewska Joanna,Bacino Carlos A.,Lalani Seema,Potocki Lorraine,Kang Sung-Hae,Patel Ankita,Cheung Sau Wai,Probst Frank J.,Graham Brett H.,Shinawi Marwan,Beaudet Arthur L.,Stankiewicz Pawel

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.21284/fullpdf

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4. Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders;Ben-Shachar;J Med Genet,2009

5. Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndrome;Carrozzo;Am J Hum Genet,1997

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