Chromosome 22q11 deletions are not found in autistic patients identified using strict diagnostic criteria

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 96, Issue 1, 2000, Pages 15-17

  Ogilvie, Caroline Mackie ^a   Moore, Janette ^b   Daker, Michael ^a   Palferman, Sarah ^b   Docherty, Zoe ^a  

^a GUY'S AND ST THOMAS' NHS FOUNDATION TRUST   (United Kingdom)

^b MEDICAL RESEARCH COUNCIL   (United Kingdom)

Author keywords

22q11 deletion; Autism; DiGeorge syndrome; Velocardiofacial syndrome

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTISM; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPING; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL;

ADOLESCENT; AUTISTIC DISORDER; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 21; FEMALE; HUMANS; INFANT, NEWBORN; MALE;

EID: 0034615155     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(20000207)96:1<15::AID-AJMG5>3.0.CO;2-M     Document Type: Article

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