Please use this identifier to cite or link to this item:
|Scopus||Web of Science®||Altmetric|
|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|
|Citation:||American Journal of Medical Genetics. Part A, 2013; 161(6):1508-1512|
|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.|
|Appears in Collections:||Obstetrics and Gynaecology publications|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.