Complex autism spectrum disorder in a patient with a 17q12 microduplication

American Journal of Medical Genetics, Part A

Volumn 158 A, Issue 5, 2012, Pages 1170-1177

  Brandt, Tracy ^a   Desai, Khyati ^a   Grodberg, David ^a   Mehta, Lakshmi ^a   Cohen, Ninette ^a   Tryfon, Ana ^a   Kolevzon, Alexander ^a   Soorya, Latha ^a   Buxbaum, Joseph D ^a   Edelmann, Lisa ^a  

^a MOUNT SINAI SCHOOL OF MEDICINE   (United States)

Author keywords

17q12 microduplication; Array CGH; Autism; Recurrent rearrangement

Indexed keywords

17Q12 MICRODUPLICATION; ARTICLE; AUTISM; CASE REPORT; CHILD; CHROMOSOME DUPLICATION; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; DIFFERENTIAL DIAGNOSIS; DNA MICROARRAY; ELECTROENCEPHALOGRAM; FACE DYSMORPHIA; FACIES; FLUORESCENCE IN SITU HYBRIDIZATION; FRAGILE X SYNDROME; GENETIC SCREENING; HUMAN; INTELLECTUAL IMPAIRMENT; MALE; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PARENTAGE ANALYSIS; PRESCHOOL CHILD; PRIORITY JOURNAL; PSYCHOLOGIC ASSESSMENT; SCORING SYSTEM; SINGLE NUCLEOTIDE POLYMORPHISM;

CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOMES, HUMAN, PAIR 17; COMPARATIVE GENOMIC HYBRIDIZATION; HUMANS; INTELLECTUAL DISABILITY; MALE; PARENTS;

EID: 84859961275     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.35267     Document Type: Article

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