Isochromosome 13 in a patient with childhood-onset schizophrenia, ADHD, and motor tic disorder

Molecular Cytogenetics

Volumn 5, Issue 1, 2012, Pages

  Graw, Sharon L ^a   Swisshelm, Karen ^a   Floyd, Kirsten ^a   Carstens, Billie J ^a   Wamboldt, Marianne Z ^a,b   Ross, Randall G ^a   Leonard, Sherry ^a,c  

^a UNIVERSITY OF COLORADO SCHOOL OF MEDICINE   (United States)

^b CHILDREN S HOSPITAL COLORADO   (United States)

^c VETERANS AFFAIRS MEDICAL CENTER   (United States)

Author keywords

Attention deficit hyperactivity disorder; childhood; Chromosome 13; Isochromosome; Schizophrenia

Indexed keywords

5 HYDROXYTRYPTAMINE RECEPTOR 2A; AMANTADINE; AMINO ACID; DEXTRO AMINO ACID OXIDASE ACTIVATOR; RISPERIDONE; SEROTONIN RECEPTOR; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; ATTENTION DEFICIT DISORDER; CASE REPORT; CENTROMERE; CHROMOSOME 13; CHRONIC MOTOR TIC DISORDER; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MUTATION; GENETIC ANALYSIS; HOMOZYGOSITY; HUMAN; HYBRIDIZATION; IMPULSIVENESS; ISOCHROMOSOME; ISOCHROMOSOME 13; KARYOTYPE; MOTOR DYSFUNCTION; ONSET AGE; PRIORITY JOURNAL; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM; VISUAL HALLUCINATION;

EID: 84855235602     PISSN: None     EISSN: 17558166     Source Type: Journal    
DOI: 10.1186/1755-8166-5-2     Document Type: Article

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