Genome sequencing identifies major causes of severe intellectual disability-Reference-Cited by-同舟云学术

Genome sequencing identifies major causes of severe intellectual disability

Published:2014-06-04 Issue:7509 Volume:511 Page:344-347
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Gilissen Christian,Hehir-Kwa Jayne Y.,Thung Djie Tjwan,van de Vorst Maartje,van Bon Bregje W. M.,Willemsen Marjolein H.,Kwint Michael,Janssen Irene M.,Hoischen Alexander,Schenck Annette,Leach Richard,Klein Robert,Tearle Rick,Bo Tan,Pfundt Rolph,Yntema Helger G.,de Vries Bert B. A.,Kleefstra Tjitske,Brunner Han G.,Vissers Lisenka E. L. M.,Veltman Joris A.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/nature13394.pdf

Reference30 articles.

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2. Mefford, H. C., Batshaw, M. L. & Hoffman, E. P. Genomics, intellectual disability, and autism. N. Engl. J. Med. 366, 733–743 (2012)

3. de Vries, B. B. et al. Diagnostic genome profiling in mental retardation. Am. J. Hum. Genet. 77, 606–616 (2005)

4. Vissers, L. E. et al. A de novo paradigm for mental retardation. Nature Genet. 42, 1109–1112 (2010)

5. Rauch, A. et al. Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study. Lancet 380, 1674–1682 (2012)

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