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Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders.
Mikhail, Fady M; Lose, Edward J; Robin, Nathaniel H; Descartes, Maria D; Rutledge, Katherine D; Rutledge, S Lane; Korf, Bruce R; Carroll, Andrew J.
Affiliation
  • Mikhail FM; Department of Genetics, University of Alabama at Birmingham, 35294, USA. fmikhail@uab.edu
Am J Med Genet A ; 155A(10): 2386-96, 2011 Oct.
Article in En | MEDLINE | ID: mdl-22031302
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Developmental Disabilities / Child Development Disorders, Pervasive / Gene Deletion / Neurogenesis / Intellectual Disability Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2011 Type: Article Affiliation country: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Developmental Disabilities / Child Development Disorders, Pervasive / Gene Deletion / Neurogenesis / Intellectual Disability Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2011 Type: Article Affiliation country: United States