A de novo 1.5 Mb microdeletion on chromosome 14q23.2-23.3 in a patient with autism and spherocytosis-Reference-Cited by-同舟云学术

A de novo 1.5 Mb microdeletion on chromosome 14q23.2-23.3 in a patient with autism and spherocytosis

Published:2011-02-28 Issue:3 Volume:4 Page:221-227
ISSN:1939-3792
Container-title:Autism Research
language:en
Short-container-title:Autism Res

Author:

Griswold Anthony J.,Ma Deqiong,Sacharow Stephanie J.,Robinson Joycelyn L.,Jaworski James M.,Wright Harry H.,Abramson Ruth K.,Lybaek Helle,Øyen Nina,Cuccaro Michael L.,Gilbert John R.,Pericak-Vance Margaret A.

Publisher

Wiley

Subject

Genetics(clinical),Clinical Neurology,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/aur.186/fullpdf

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2. Autism Genetics Resource Exchange 2008 http://www.agre.org/

3. Autism as a strongly genetic disorder: Evidence from a British twin study;Bailey;Psychological Medicine,1995

4. Beta spectrin kissimmee: A spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1;Becker;The Journal of Clinical Investigation,1993

5. MECP2 mutations account for most cases of typical forms of Rett syndrome;Bienvenu;Human Molecular Genetics,2000

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