Neurodevelopmental disorders among individuals with duplication of 4p13 to 4p12 containing a GABA A receptor subunit gene cluster

European Journal of Human Genetics

Volumn 22, Issue 1, 2014, Pages 105-109

  Polan, Michelle B ^a   Pastore, Matthew T ^a,b   Steingass, Katherine ^a,b   Hashimoto, Sayaka ^a   Thrush, Devon L ^a,b   Pyatt, Robert ^a,b   Reshmi, Shalini ^a,b   Gastier Foster, Julie M ^a,b   Astbury, Caroline ^a,b   McBride, Kim L ^a,b  

^a NATIONWIDE CHILDREN S HOSPITAL   (United States)

^b OHIO STATE UNIVERSITY   (United States)

Author keywords

autism; bipolar disorder; chromosome disorders; DNA copy number variation; intellectual disabilities

Indexed keywords

4 AMINOBUTYRIC ACID A RECEPTOR;

APRAXIA; ARTICLE; ATTENTION DEFICIT DISORDER; AUTISM; BIPOLAR DISORDER; CASE REPORT; CHILD; CHROMOSOME 4P; CHROMOSOME DUPLICATION; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; DEVELOPMENTAL DISORDER; DYSLEXIA; FAMILY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE CLUSTER; GENE DUPLICATION; GENETIC SUSCEPTIBILITY; HUMAN; INTELLECTUAL IMPAIRMENT; LEARNING DISORDER; MALE; PRIORITY JOURNAL; SCHOOL CHILD; SPEECH DELAY; SPEECH THERAPY; ADULT; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHROMOSOME 4; DEVELOPMENTAL DISABILITIES; FEMALE; GENETICS; PATHOLOGY; PEDIGREE; PHENOTYPE; PRESCHOOL CHILD;

ADULT; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 4; COMPARATIVE GENOMIC HYBRIDIZATION; DEVELOPMENTAL DISABILITIES; DNA COPY NUMBER VARIATIONS; FEMALE; GENE DUPLICATION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; PEDIGREE; PHENOTYPE; RECEPTORS, GABA-A;

EID: 84890803201     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2013.99     Document Type: Article

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