SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delay

American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

Volumn 162, Issue 8, 2013, Pages 832-840

  An, Yu ^a,b   Amr, Sami S ^c,d,e   Torres, Alcy ^b,c   Weissman, Laura ^b,c   Raffalli, Peter ^b,c   Cox, Gerald ^b,c   Sheng, Xiaoming ^b   Lip, Va ^b   Bi, Weimin ^f   Patel, Ankita ^f   Stankiewicz, Pawel ^f   Wu, Bai Lin ^a,b,c   Shen, Yiping ^b,c,g  

^a FUDAN UNIVERSITY   (China)

^b BOSTON CHILDREN S HOSPITAL   (United States)

^c HARVARD MEDICAL SCHOOL   (United States)

^d BRIGHAM AND WOMEN S HOSPITAL   (United States)

^e LABORATORY FOR MOLECULAR MEDICINE   (United States)

^f BAYLOR COLLEGE OF MEDICINE   (United States)

^g SHANGHAI JIAO TONG UNIVERSITY SCHOOL OF MEDICINE   (China)

Author keywords

20p13; Developmental delay; Microdeletion; NRSN2; SOX12

Indexed keywords

ADOLESCENT; AGGRESSION; AMBLYOPIA; ANTERIOR FONTANEL; ANTEVERTED NOSTRIL; ARTICLE; ASTHMA; ASTIGMATISM; ATTENTION DEFICIT DISORDER; AUTISM; AUTISM DIAGNOSTIC OBSERVATION SCHEDULE; AUTOMUTILATION; AUTOSOME; BAYLEY SCALES OF INFANT DEVELOPMENT; CAUCASIAN; CHILD; CHILD REARING; CHROMOSOME 20P13; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; COGNITIVE DEFECT; COLOR BLINDNESS; COMMUNICATION DISORDER; COMPARATIVE GENOMIC HYBRIDIZATION; CONCEPT FORMATION; CRYPTORCHISM; DEVELOPMENTAL DISORDER; DEVELOPMENTAL LANGUAGE DISORDER; DIARRHEA; DYSARTHRIA; ELECTROENCEPHALOGRAPHY; FEMALE; FOOT MALFORMATION; GENE; GENE EXPRESSION; GENETIC ASSOCIATION; GENITAL MALFORMATION; HIGH ARCHED PALATE; HUMAN; HYPERNASALITY; INTELLECTUAL IMPAIRMENT; INTELLIGENCE QUOTIENT; LANDAU KLEFFNER SYNDROME; LANGUAGE DELAY; MACROCEPHALY; MALE; MEDICAL HISTORY; MICROARRAY ANALYSIS; MICROTIA; MOTOR PERFORMANCE; MUSCLE HYPERTONIA; NAIL HYPOPLASIA; NRSN2 GENE; OBSESSIVE COMPULSIVE DISORDER; PALPEBRAL FISSURE ANOMALY; PERVASIVE DEVELOPMENTAL DISORDER NOT OTHERWISE SPECIFIED; PHYSICAL EXAMINATION; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SLEEP DISORDER; SOX12 GENE; SPEECH DELAY; STRUCTURED QUESTIONNAIRE; TIC; TOOTH DISEASE; WECHSLER INTELLIGENCE SCALE;

20P13; DEVELOPMENTAL DELAY; MICRODELETION; NRSN2; SOX12;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 20; COMPARATIVE GENOMIC HYBRIDIZATION; DEVELOPMENTAL DISABILITIES; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; HUMANS; MALE; MEMBRANE PROTEINS; SOXC TRANSCRIPTION FACTORS;

EID: 84887031838     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.32187     Document Type: Article

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