Progress in cytogenetics: Implications for child psychopathology

Journal of the American Academy of Child and Adolescent Psychiatry

Volumn 49, Issue 8, 2010, Pages 736-751

  Hoffman, Ellen J ^a   State, Matthew W ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

autism; childhood onset schizophrenia; genetics; structural chromosomal variation; Tourette syndrome

Indexed keywords

CONTACTIN; DISRUPTED IN SCHIZOPHRENIA 1 PROTEIN; F BOX PROTEIN; METHYL CPG BINDING PROTEIN 2; NEUREXIN; NEUROLIGIN; PARKIN;

ASPERGER SYNDROME; ATTENTION DEFICIT DISORDER; AUTISM; CHILD PSYCHIATRY; CHILDHOOD DISEASE; CHILDHOOD ONSET SCHIZOPHRENIA; CHROMOSOME; CHROMOSOME 16P; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME STRUCTURE; COGNITIVE DEFECT; COPY NUMBER VARIATION; CYTOGENETICS; DNA SEQUENCE; FRAGILE X SYNDROME; GENE MUTATION; GENETIC RISK; GENETIC VARIABILITY; GILLES DE LA TOURETTE SYNDROME; HAPPY PUPPET SYNDROME; HUMAN; MENTAL DISEASE; MICROARRAY ANALYSIS; MICROSCOPY; NERVE CELL DIFFERENTIATION; NONHUMAN; OBSESSIVE COMPULSIVE DISORDER; PRADER WILLI SYNDROME; PRIORITY JOURNAL; REVIEW; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CYTOGENETICS; FORECASTING; GENETIC VARIATION; HUMANS; MENTAL DISORDERS; PSYCHOPATHOLOGY; SCHIZOPHRENIA; SCHIZOPHRENIC PSYCHOLOGY; TOURETTE SYNDROME;

EID: 77955681110     PISSN: 08908567     EISSN: 15275418     Source Type: Journal    
DOI: 10.1016/j.jaac.2010.03.016     Document Type: Review

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