Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome-Reference-Cited by-同舟云学术

Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome

Published:2012-04-29 Issue:6 Volume:44 Page:639-641
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Koolen David A,Kramer Jamie M,Neveling Kornelia,Nillesen Willy M,Moore-Barton Heather L,Elmslie Frances V,Toutain Annick,Amiel Jeanne,Malan Valérie,Tsai Anne Chun-Hui,Cheung Sau Wai,Gilissen Christian,Verwiel Eugene T P,Martens Sarah,Feuth Ton,Bongers Ernie M H F,de Vries Petra,Scheffer Hans,Vissers Lisenka E L M,de Brouwer Arjan P M,Brunner Han G,Veltman Joris A,Schenck Annette,Yntema Helger G,de Vries Bert B A

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2262.pdf

Reference14 articles.

1. Koolen, D.A. et al. Nat. Genet. 38, 999–1001 (2006).

2. Sharp, A.J. et al. Nat. Genet. 38, 1038–1042 (2006).

3. Shaw-Smith, C. et al. Nat. Genet. 38, 1032–1037 (2006).

4. Koolen, D.A. et al. J. Med. Genet. 45, 710–720 (2008).

5. Tan, T.Y. et al. J. Med. Genet. 46, 480–489 (2009).

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