Ring chromosome 22 and autism: Report and review

American Journal of Medical Genetics

Volumn 90, Issue 5, 2000, Pages 382-385

  MacLean, Joanna E ^a   Teshima, Ikuko E ^b   Szatmari, Peter ^c   Nowaczyk, Małgorzata J M ^a,c,d  

^a MCMASTER UNIVERSITY   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

^c MCMASTER UNIVERSITY   (Canada)

^d MCMASTER UNIVERSITY MEDICAL CENTRE   (Canada)

Author keywords

2 3 toe syndactyly; Autism; Ring chromosome 22

Indexed keywords

ARTICLE; AUTISM; CASE REPORT; CHILD; CHROMOSOME 22; CHROMOSOME ANALYSIS; CLINICAL FEATURE; DISEASE ASSOCIATION; HUMAN; KARYOTYPING; MALE; PHENOTYPE; PRIORITY JOURNAL; RING CHROMOSOME; SYNDACTYLY;

ABNORMALITIES, MULTIPLE; AUTISTIC DISORDER; CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 22; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; RING CHROMOSOMES;

EID: 0034723727     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(20000228)90:5<382::AID-AJMG7>3.0.CO;2-T     Document Type: Article

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