Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families-Reference-Cited by-同舟云学术

Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families

Published:2017-04-11 Issue:4 Volume:23 Page:973-984
ISSN:1359-4184
Container-title:Molecular Psychiatry
language:en
Short-container-title:Mol Psychiatry

Author:

Harripaul R^ORCID,Vasli N,Mikhailov A,Rafiq M A,Mittal K,Windpassinger C,Sheikh T I,Noor A,Mahmood H,Downey S,Johnson M,Vleuten K,Bell L,Ilyas M,Khan F S,Khan V,Moradi M,Ayaz M,Naeem F,Heidari A,Ahmed I,Ghadami S,Agha Z,Zeinali S,Qamar R,Mozhdehipanah H,John P,Mir A,Ansar M,French L,Ayub M,Vincent J B

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Molecular Biology

Link

http://www.nature.com/articles/mp201760.pdf

Reference90 articles.

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3. Ropers H-H, Hamel BC . X-linked mental retardation. Nat Rev Genet 2005; 6: 46–57.

4. de Ligt J, Willemsen MH, van Bon BW, Kleefstra T, Yntema HG, Kroes T et al. Diagnostic exome sequencing in persons with severe intellectual disability. N Engl J Med 2012; 367: 1921–1929.

5. Hamdan FF, Srour M, Capo-Chichi J-M, Daoud H, Nassif C, Patry L et al. De novo mutations in moderate or severe intellectual disability. PLoS Genet 2014; 10: e1004772.

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