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De novo intragenic deletion of the autism susceptibility candidate 2 (AUTS2) gene in a patient with developmental delay: a case report and literature review.
Jolley, Alexandra; Corbett, Mark; McGregor, Lesley; Waters, Wendy; Brown, Susan; Nicholl, Jillian; Yu, Sui.
Affiliation
  • Jolley A; Department of Genetic Medicine, Directorate of Genetics and Molecular Pathology, SA Pathology at Women's and Children's Hospital, and School of Paediatrics and Reproductive Health, The University of Adelaide, North Adelaide, South Australia, Australia.
Am J Med Genet A ; 161A(6): 1508-12, 2013 Jun.
Article in En | MEDLINE | ID: mdl-23650183
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Autistic Disorder / Proteins / Developmental Disabilities / Chromosome Deletion Limits: Adolescent / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2013 Document type: Article Affiliation country: Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Autistic Disorder / Proteins / Developmental Disabilities / Chromosome Deletion Limits: Adolescent / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2013 Document type: Article Affiliation country: Country of publication: