Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation

Journal of Medical Genetics

Volumn 50, Issue 3, 2013, Pages 163-173

  Handrigan, Gregory Ryan ^a   Chitayat, David ^b,c   Lionel, Anath C ^a,d   Pinsk, Maury ^e   Vaags, Andrea K ^d   Marshall, Christian R ^a,d   Dyack, Sarah ^f   Escobar, Luis F ^g   Fernandez, Bridget A ^h   Stegman, Joseph C ⁱ   Rosenfeld, Jill A ^j   Shaffer, Lisa G ^j   Goodenberger, McKinsey ^k   Hodge, Jennelle C ^k   Cain, Jason E ^b   Babul Hirji, Riyana ^b   Stavropoulos, Dimitri J ^a,b   Yiu, Verna ^e   Scherer, Stephen W ^a,d   Rosenblum, Norman D ^a,b,l  

^a UNIVERSITY OF TORONTO   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

^c MOUNT SINAI HOSPITAL   (Canada)

^d HOSPITAL FOR SICK CHILDREN   (Canada)

^e UNIVERSITY OF ALBERTA   (Canada)

^f DALHOUSIE UNIVERSITY   (Canada)

^g Peyton Manning Children's Hospital   (United States)

^h MEMORIAL UNIVERSITY OF NEWFOUNDLAND   (Canada)

ⁱ Developmental and Behavioral Clinic of the Carolinas   (United States)

^j PERKINELMER INC   (United States)

^k MAYO CLINIC   (United States)

^l UNIVERSITY OF TORONTO   (Canada)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ANKRD11 GENE; ARTICLE; AUTISM; CHILD; CHROMOSOME 16Q; CHROMOSOME DELETION; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; FBX031 GENE; FEMALE; FOXF1 GENE; GENE; GENETIC ASSOCIATION; GENOTYPE; HUMAN; HYDRONEPHROSIS; INTELLECTUAL IMPAIRMENT; KIDNEY MALFORMATION; MALE; MICROARRAY ANALYSIS; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; ZCCHC14 GENE;

ADOLESCENT; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHILD, PRESCHOOL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 16; DNA COPY NUMBER VARIATIONS; FEMALE; GENE DELETION; HUMANS; INFANT; INFANT, NEWBORN; INTELLECTUAL DISABILITY; KIDNEY; MALE; REPRESSOR PROTEINS; YOUNG ADULT;

EID: 84874763714     PISSN: 00222593     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmedgenet-2012-101288     Document Type: Article

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