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https://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. |
DOI: | 10.1002/ajmg.a.35922 |
Published version: | http://dx.doi.org/10.1002/ajmg.a.35922 |
Appears in Collections: | Aurora harvest 4 Obstetrics and Gynaecology publications |
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