Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autism-Reference-Cited by-同舟云学术

Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autism

Published:2016-11-15 Issue:2 Volume:136 Page:179-192
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Bramswig Nuria C.^ORCID,Lüdecke H.-J.,Pettersson M.,Albrecht B.,Bernier R. A.,Cremer K.,Eichler E. E.,Falkenstein D.,Gerdts J.,Jansen S.,Kuechler A.,Kvarnung M.,Lindstrand A.,Nilsson D.,Nordgren A.,Pfundt R.,Spruijt L.,Surowy H. M.,de Vries B. B. A.,Wieland T.,Engels H.,Strom T. M.,Kleefstra T.,Wieczorek D.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-016-1743-x.pdf

Reference24 articles.

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5. de Ligt J et al (2012) Diagnostic exome sequencing in persons with severe intellectual disability. N Engl J Med 367:1921–1929. doi: 10.1056/NEJMoa1206524

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