A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk-Reference-Cited by-同舟云学术

A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk

Published:2010-08-22 Issue:9 Volume:42 Page:745-750
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Antonacci Francesca,Kidd Jeffrey M,Marques-Bonet Tomas,Teague Brian,Ventura Mario,Girirajan Santhosh,Alkan Can,Campbell Catarina D,Vives Laura,Malig Maika,Rosenfeld Jill A,Ballif Blake C,Shaffer Lisa G,Graves Tina A,Wilson Richard K,Schwartz David C,Eichler Evan E

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.643.pdf

Reference52 articles.

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3. Conrad, D.F. et al. Origins and functional impact of copy number variation in the human genome. Nature 464, 704–712 (2010).

4. Cheung, V.G. et al. Integration of cytogenetic landmarks into the draft sequence of the human genome. Nature 409, 953–958 (2001).

5. Bailey, J.A. et al. Recent segmental duplications in the human genome. Science 297, 1003–1007 (2002).

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