Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/78852
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Type: Journal article
Title: De novo intragenic deletion of the autism susceptibility candidate 2 (AUTS2) gene in a patient with developmental delay: A case report and literature review
Author: Jolley, A.
Corbett, M.
McGregor, L.
Waters, W.
Brown, S.
Nicholl, J.
Yu, S.
Citation: American Journal of Medical Genetics. Part A, 2013; 161(6):1508-1512
Publisher: Wiley-Liss
Issue Date: 2013
ISSN: 1552-4825
1552-4833
Statement of
Responsibility: 
Alexandra Jolley, Mark Corbett, Lesley McGregor, Wendy Waters, Susan Brown, Jillian Nicholl, and Sui Yu
Keywords: Humans; Chromosome Deletion; Translocation, Genetic; Proteins; Cytoskeletal Proteins; Transcription Factors; In Situ Hybridization, Fluorescence; Autistic Disorder; Developmental Disabilities; Base Sequence; Adolescent; Male; Comparative Genomic Hybridization; Chromosome Inversion
Rights: Copyright © 2013 Wiley Periodicals, Inc.
RMID: 0020128894
DOI: 10.1002/ajmg.a.35922
Appears in Collections:Obstetrics and Gynaecology publications

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