Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?-Reference-Cited by-同舟云学术

Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?

Published:2012-08-22 Issue:7 Volume:159B Page:812-822
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Van Den Bossche Maarten J.,Johnstone Mandy,Strazisar Mojca,Pickard Benjamin S.,Goossens Dirk,Lenaerts An-Sofie,De Zutter Sonia,Nordin Annelie,Norrback Karl-Fredrik,Mendlewicz Julien,Souery Daniel,De Rijk Peter,Sabbe Bernard G.,Adolfsson Rolf,Blackwood Douglas,Del-Favero Jurgen

Publisher

Wiley

Subject

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

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.b.32088/fullpdf

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4. Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders;Ching;Am J Med Genet Part B,2010

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