Genetic variation in the 22q11 locus and susceptibility to schizophrenia

Proceedings of the National Academy of Sciences of the United States of America

Volumn 99, Issue 26, 2002, Pages 16859-16864

  Liu, Hui ^a   Abecasis, Gonçalo R ^b   Heath, Simon C ^c   Knowles, Alyson ^a   Demars, Sandra ^a   Chen, Ying Jiun ^d   Roos, J Louw ^e   Rapoport, Judith L ^f   Gogos, Joseph A ^d   Karayiorgou, Maria ^a  

^a ROCKEFELLER UNIVERSITY   (United States)

^b UNIVERSITY OF MICHIGAN   (United States)

^c MEMORIAL SLOAN KETTERING CANCER CENTER   (United States)

^d Department of Physiology ^*  (United States)

^e UNIVERSITY OF PRETORIA   (South Africa)

^f NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHROMOSOME 22Q; CONTROLLED STUDY; FAMILY STUDY; GENE DELETION; GENETIC LINKAGE; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MARKER GENE; POLYMORPHIC LOCUS; POPULATION RESEARCH; PRIORITY JOURNAL; RESTRICTION MAPPING; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM;

AMINO ACID SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 22; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LINKAGE DISEQUILIBRIUM; MOLECULAR SEQUENCE DATA; POLYMORPHISM, SINGLE NUCLEOTIDE; SCHIZOPHRENIA; VARIATION (GENETICS);

EID: 0037168523     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.232186099     Document Type: Article

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