Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

Journal of Medical Genetics

Volumn 46, Issue 4, 2009, Pages 242-248

  Miller, D T ^a,b,c   Shen, Y ^a,b,c,d   Weiss, L A ^b,c,d,e   Korn, J ^d,e   Anselm, I ^a,b   Bridgemohan, C ^a,b   Cox, G F ^a,b,f   Dickinson, H ^a   Gentile, J ^a,b   Harris, D J ^a,b   Hegde, V ^a,b   Hundley, R ^a,b   Khwaja, O ^a,b,c   Kothare, S ^a,b   Luedke, C ^a,b   Nasir, R ^a,b,c   Poduri, A ^a,b   Prasad, K ^a,b   Raffalli, P ^a,b   Reinhard, A ^a   Smith, S E ^a,b,f   Sobeih, M M ^a,b,c   Soul, J S ^a,b   Stoler, J ^a,b   Takeoka, M ^a,b   Tan, W H ^a,b   Thakuria, J ^a,b   Wolff, R ^a,b   Yusupov, R ^a,b   Gusella, J F ^b,c,d,e   Daly, M J ^b,c,d,e   Wu, B L ^a,b,c   more..

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

^c Autism Consortium Inc   (United States)

^d MASSACHUSETTS GENERAL HOSPITAL   (United States)

^e BROAD INSTITUTE OF MIT AND HARVARD   (United States)

^f GENZYME CORPORATION   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BUNGAROTOXIN RECEPTOR; DNA; MICRORNA;

ADULT; ANXIETY DISORDER; ARTICLE; ATTENTION DEFICIT DISORDER; AUTISM; CHILD; CHROMOSOME 15Q; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CLINICAL ARTICLE; COGNITIVE DEFECT; COMPARATIVE GENOMIC HYBRIDIZATION; DEVELOPMENTAL DISORDER; DNA DETERMINATION; ELECTROENCEPHALOGRAM; FEMALE; HUMAN; INTELLIGENCE QUOTIENT; LANGUAGE DISABILITY; LEARNING DISORDER; MALE; MENTAL DEFICIENCY; MENTAL PATIENT; MOOD DISORDER; PHENOTYPE; PRIORITY JOURNAL; SEIZURE;

ADOLESCENT; AUTISTIC DISORDER; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 15; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; GENE DUPLICATION; HUMANS; INFANT; MALE; MENTAL RETARDATION; PHENOTYPE; YOUNG ADULT;

EID: 65949085347     PISSN: 00222593     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2008.059907     Document Type: Article

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