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

Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype

Published:2012-04-29 Issue:6 Volume:44 Page:636-638
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Zollino Marcella,Orteschi Daniela,Murdolo Marina,Lattante Serena,Battaglia Domenica,Stefanini Chiara,Mercuri Eugenio,Chiurazzi Pietro,Neri Giovanni,Marangi Giuseppe

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2257.pdf

Reference15 articles.

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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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