15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH

Clinical Genetics

Volumn 69, Issue 2, 2006, Pages 124-134

  Koochek, M ^a,c   Harvard, C ^a,c   Hildebrand, M J ^a,c   Van Allen, M ^a   Wingert, H ^a,c   Mickelson, E ^a,c   Holden, J J A ^b,c   Rajcan Separovic, E ^a,c   Lewis, M E Suzanne ^a,c  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^b QUEEN S UNIVERSITY   (Canada)

^c Autism Spectrum Disorders Canadian American Research Consortium   (Canada)

Author keywords

Autism spectrum disorder (ASD); Chromosome 6q, 14q, 15q; Comparative genomic hybridization (CGH); Cryptic translocation; Fluorescent in situ hybridization (FISH); Intellectual disability; Microarray; Microdeletion; Microduplication

Indexed keywords

ACROCENTRIC CHROMOSOME; ADULT; ARTICLE; AUTISM; CHILD; CHROMOSOME 14; CHROMOSOME 14Q; CHROMOSOME 15; CHROMOSOME 15Q; CHROMOSOME DUPLICATION; CHROMOSOME SEGREGATION; CHROMOSOME TRANSLOCATION 14; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; CYTOGENETICS; DISEASE ASSOCIATION; EXTRACHROMOSOMAL INHERITANCE; FAMILY STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; KARYOTYPE; MALE; MARKER CHROMOSOME; MOLECULAR PROBE; PATHOGENESIS; PRIORITY JOURNAL; RECURRENCE RISK; SUPERNUMERARY CHROMOSOME;

ADOLESCENT; ADULT; AUTISTIC DISORDER; CHILD; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 14; CHROMOSOMES, HUMAN, PAIR 15; FAMILY HEALTH; FEMALE; GENE DUPLICATION; GENOME, HUMAN; GENOMICS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; MALE; NUCLEIC ACID HYBRIDIZATION; PEDIGREE; TRANSLOCATION, GENETIC;

EID: 33644851753     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2005.00560.x     Document Type: Article

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