Large, rare chromosomal deletions associated with severe early-onset obesity-Reference-Cited by-同舟云学术

Large, rare chromosomal deletions associated with severe early-onset obesity

Published:2009-12-06 Issue:7281 Volume:463 Page:666-670
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Bochukova Elena G.,Huang Ni,Keogh Julia,Henning Elana,Purmann Carolin,Blaszczyk Kasia,Saeed Sadia,Hamilton-Shield Julian,Clayton-Smith Jill,O’Rahilly Stephen,Hurles Matthew E.,Farooqi I. Sadaf

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/nature08689.pdf

Reference25 articles.

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3. Weiss, L. A. et al. Association between microdeletion and microduplication at 16p11.2 and autism. N. Engl. J. Med. 358, 667–675 (2008)

4. Marshall, C. R. et al. Structural variation of chromosomes in autism spectrum disorder. Am. J. Hum. Genet. 82, 477–488 (2008)

5. Bijlsma, E. K. et al. Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals. Eur. J. Med. Genet. 52, 77–87 (2009)

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