Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: Identification of candidate genes for autism and of homologous dna segments in 15q22-q23 and 15q11-q13

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 96, Issue 6, 2000, Pages 765-770

  Smith, Moyra ^a   Filipek, Pauline A ^a   Wu, Charles ^a   Bocian, Maureen ^a   Hakim, Simin ^a   Modahl, Charlotte ^a   Anne Spence, M ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

15q11 q13; 15q22 q23; Autism; PTPN9; SLP 1 hUNC24

Indexed keywords

PROTEIN TYROSINE PHOSPHATASE;

ARTICLE; AUTISM; CASE REPORT; CHROMOSOME 15Q; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; DELETION MUTANT; DEVELOPMENTAL DISORDER; DNA SEQUENCE; FACE DYSMORPHIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION; HUMAN; HYBRIDIZATION; PRESCHOOL CHILD; PRIORITY JOURNAL;

EID: 0034606205     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/1096-8628(20001204)96:6<765::aid-ajmg13>3.0.co;2-l     Document Type: Article

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