Screening for 22q11 deletions in a schizophrenia population

Schizophrenia Research

Volumn 52, Issue 3, 2001, Pages 167-170

  Arinami, T ^a   Ohtsuki, T ^a   Takase, K ^a   Shimizu, H ^b   Yoshikawa, T ^c   Horigome, H ^a   Nakayama, J ^a   Toru, M ^d  

^a UNIVERSITY OF TSUKUBA   (Japan)

^b Hokushin General Hospital   (Japan)

^c RIKEN BRAIN SCIENCE INSTITUTE   (Japan)

^d TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

Author keywords

Chromosome 22q11; FISH; Microsatellite; Schizophrenia; Velocardiofacial syndrome

Indexed keywords

DNA MARKER; MICROSATELLITE DNA;

ADULT; AGED; ARTICLE; CHROMOSOME ANALYSIS; CONTROLLED STUDY; DISEASE SEVERITY; FACE MALFORMATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE FREQUENCY; GENETIC SCREENING; GENOTYPE; HUMAN; JAPAN; MAJOR CLINICAL STUDY; MALE; MENTAL DEFICIENCY; PRIORITY JOURNAL; RACE; SCHIZOPHRENIA; VELOCARDIOFACIAL SYNDROME;

ADULT; AGED; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; GENE DELETION; GENETIC PREDISPOSITION TO DISEASE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; JAPAN; LINKAGE DISEQUILIBRIUM; MALE; MICROSATELLITE REPEATS; MIDDLE AGED; SCHIZOPHRENIA;

EID: 0035575466     PISSN: 09209964     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0920-9964(00)00192-4     Document Type: Article

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