A novel 3q29 deletion associated with autism, intellectual disability, psychiatric disorders, and obesity

American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

Volumn 171, Issue 2, 2016, Pages 290-299

  Biamino, Elisa ^a   di Gregorio, Eleonora ^b   Belligni, Elga Fabia ^a   Keller, Roberto ^c   Riberi, Evelise ^a   Gandione, Marina ^a   Calcia, Alessandro ^d   Mancini, Cecilia ^d   Giorgio, Elisa ^d   Cavalieri, Simona ^b,d   Pappi, Patrizia ^b   Talarico, Flavia ^b   Fea, Antonio M ^d   de Rubeis, Silvia ^e   Cirillo Silengo, Margherita ^a   Ferrero, Giovanni Battista ^a   Brusco, Alfredo ^b,d  

^a UNIVERSITY OF TURIN   (Italy)

^b CITTÀ DELLA SALUTE E DELLA SCIENZA HOSPITAL   (Italy)

^c Unit of Pneumology   (Italy)

^d UNIVERSITY OF TURIN   (Italy)

^e MOUNT SINAI SCHOOL OF MEDICINE   (United States)

Author keywords

Autistic spectrum disorder; Contiguous gene syndrome; Intellectual disability; Obesity; Schizophrenia

Indexed keywords

ADULT; AGED; ANXIETY DISORDER; ARTICLE; ATP13A4 GENE; AUTISM; CENTROMERE; CHILD; CHROMOSOME 3Q; CHROMOSOME DELETION; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; GENE; HAPLOINSUFFICIENCY; HES1 GENE; HUMAN; INTELLECTUAL IMPAIRMENT; MAJOR DEPRESSION; MENTAL DISEASE; MIDDLE AGED; OBESITY; OPA1 GENE; OPTIC NERVE ATROPHY; PERSONALITY DISORDER; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHIZOPHRENIA; SCHOOL CHILD; CASE REPORT; CHROMOSOME 3; COMPLICATION; GENETICS; INFANT; MALE; NEWBORN; PEDIGREE; PHENOTYPE; POLYMERASE CHAIN REACTION; PSYCHOSIS;

ADULT; AGED; AUTISTIC DISORDER; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 3; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; INTELLECTUAL DISABILITY; MALE; MIDDLE AGED; OBESITY; PEDIGREE; PHENOTYPE; POLYMERASE CHAIN REACTION; PSYCHOTIC DISORDERS;

EID: 84958161380     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.32406     Document Type: Article

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