High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy

BMC Medical Genetics

Volumn 12, Issue , 2011, Pages

  Stewart, Larissa R ^a   Hall, April L ^a   Kang, Sung Hae L ^a   Shaw, Chad A ^a   Beaudet, Arthur L ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BIPOLAR DISORDER; CHROMOSOME 15Q; COMORBIDITY; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; DNA DETERMINATION; EPILEPSY; FEMALE; GENE DELETION; GENE DOSAGE; GENE DUPLICATION; GENE FREQUENCY; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; HUMAN; MAJOR CLINICAL STUDY; MALE; NEUROPATHOLOGY; SCHIZOPHRENIA; CASE CONTROL STUDY; CHROMOSOME 1; CHROMOSOME 15; CHROMOSOME 22; CHROMOSOME DELETION; CHROMOSOME DISORDER; CHROMOSOME DUPLICATION; COPY NUMBER VARIATION; GENETICS; TRISOMY;

BIPOLAR DISORDER; CASE-CONTROL STUDIES; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOME DUPLICATION; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, PAIR 22; COMPARATIVE GENOMIC HYBRIDIZATION; DNA COPY NUMBER VARIATIONS; EPILEPSY; FEMALE; HUMANS; MALE; SCHIZOPHRENIA; TRISOMY;

EID: 82055181692     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-12-154     Document Type: Article

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