Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism

American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

Volumn 144, Issue 7, 2007, Pages 869-876

  Martin, Christa Lese ^a   Duvall, Jacqueline A ^b   Ilkin, Yesim ^c   Simon, Jason S ^d   Arreaza, M Gladys ^d   Wilkes, Kristin ^b   Alvarez Retuerto, Ana ^b   Whichello, Amy ^e   Powell, Cynthia M ^f   Rao, Kathleen ^f   Cook, Edwin ^g   Geschwind, Daniel H ^b  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITY OF CHICAGO   (United States)

^d MERCK RESEARCH LABORATORIES   (United States)

^e DUKE UNIVERSITY   (United States)

^f UNIVERSITY OF NORTH CAROLINA   (United States)

^g UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

Author keywords

Association analysis; Copy number variation; Cytogenetic imbalance; RNA binding; Splicing factor

Indexed keywords

ATAXIN 2 BINDING PROTEIN 1; MESSENGER RNA; PROTEIN; UNCLASSIFIED DRUG;

A2BP1 GENE; ARTICLE; AUTISM; CASE REPORT; CHILD; CHROMOSOME 15P; CHROMOSOME 16P; CHROMOSOME TRANSLOCATION 15; CHROMOSOME TRANSLOCATION 16; CYTOGENETICS; DEVELOPMENTAL DISORDER; EPILEPSY; EXON; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FOX1 GENE; GENE; GENE DELETION; GENE MUTATION; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; INTRON; LYMPHOCYTE; MOLECULAR GENETICS; PRIORITY JOURNAL; PROMOTER REGION; REAL TIME POLYMERASE CHAIN REACTION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

AUTISTIC DISORDER; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, PAIR 7; CYTOGENETIC ANALYSIS; EPILEPSY; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MENTAL RETARDATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN ISOFORMS; RNA-BINDING PROTEINS; TRANSLOCATION, GENETIC;

EID: 35148885611     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.30530     Document Type: Article

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