22q11 deletion syndrome in childhood onset schizophrenia: An update

Molecular Psychiatry

Volumn 9, Issue 3, 2004, Pages 225-226+221

  Sporn, A ^a   Addington, A ^a   Reiss, A L ^b   Dean, M ^c   Gogtay, N ^a   Potocnik, U ^c   Greenstein, D ^a   Hallmayer, J ^b   Gochman, P ^a   Lenane, M ^a   Baker, N ^a   Tossell, J ^a   Rapoport, J L ^a  

^a NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

^b STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c NATIONAL CANCER INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CLOZAPINE; NEUROLEPTIC AGENT; OLANZAPINE; QUETIAPINE;

ARTICLE; CHILDHOOD DISEASE; CHROMOSOME 22Q; CHROMOSOME DELETION; CYTOGENETICS; DIAGNOSTIC APPROACH ROUTE; ELECTROENCEPHALOGRAPHY; EPILEPTIC DISCHARGE; FLUORESCENCE IN SITU HYBRIDIZATION; FREQUENCY ANALYSIS; GENE AMPLIFICATION; GENETIC ASSOCIATION; GENETIC CORRELATION; GENETIC LOAD; GENETIC SCREENING; HUMAN; INCIDENCE; NEUROBIOLOGY; PATERNITY; POPULATION GENETICS; PREVALENCE; PRIORITY JOURNAL; SCHIZOPHRENIA; STATISTICAL SIGNIFICANCE; TREATMENT INDICATION;

ADOLESCENT; AGE OF ONSET; CHILD; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 22; HUMANS; SCHIZOPHRENIA;

EID: 11144354655     PISSN: 13594184     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.mp.4001477     Document Type: Article

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