A girl with pervasive developmental disorder and complex chromosome rearrangement involving 8p and 10p

Journal of Autism and Developmental Disorders

Volumn 35, Issue 3, 2005, Pages 393-399

  Zwaigenbaum, L ^a   Sonnenberg, L K ^a   Heshka, T ^a   Eastwood, S ^a   Xu, J ^a,b  

^a MCMASTER UNIVERSITY   (Canada)

^b LONDON HEALTH SCIENCES CENTRE   (Canada)

Author keywords

10p translocation; 8p translocation and insertion; Complex chromosome rearrangement; Pervasive developmental disorder

Indexed keywords

ARTICLE; AUTISM; CASE REPORT; CHROMOSOME 10P; CHROMOSOME 8P; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; DEVELOPMENTAL DISORDER; FACIES; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; HUMAN; JOINT LAXITY; KARYOTYPE; PALATE; PALATOPHARYNGEAL INCOMPETENCE; PRESCHOOL CHILD; PRIORITY JOURNAL; SOCIAL INTERACTION; SPEECH DISORDER; STATISTICAL SIGNIFICANCE; STRABISMUS;

CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 8; FEMALE; GENE REARRANGEMENT; HUMANS; KARYOTYPING; TRANSLOCATION, GENETIC;

EID: 23744514147     PISSN: 01623257     EISSN: 15733432     Source Type: Journal    
DOI: 10.1007/s10803-005-3307-0     Document Type: Article

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