An extended genome scan in 442 Canadian multiple sclerosis-affected sibships: A report from the Canadian Collaborative Study Group

Human Molecular Genetics

Volumn 13, Issue 10, 2004, Pages 1005-1015

  Dyment, David A ^a   Sadovnick, A Dessa ^b   Willer, Cristen J ^a   Armstrong, Holly ^c   Cader, Zameel M ^a   Wiltshire, Steven ^a   Kalman, Bernadette ^d   Risch, Neil ^e   Ebers, George C ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^c UNIVERSITY OF WESTERN ONTARIO   (Canada)

^d Och Spine at New York Presbyterian Hospitals   (United States)

^e STANFORD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HLA DR ANTIGEN;

ALLELE; ARTICLE; CANADA; CHROMOSOME 11P; CHROMOSOME 12Q; CHROMOSOME 17Q; CHROMOSOME 18P; CHROMOSOME 18Q; CHROMOSOME 1P; CHROMOSOME 21Q; CHROMOSOME 2Q; CHROMOSOME 5P; CHROMOSOME 6P; CHROMOSOME 9Q; CHROMOSOME REPLICATION; CONTROLLED STUDY; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC PREDISPOSITION; GENETIC SCREENING; GENOTYPE; HLA TYPING; HUMAN; MAJOR CLINICAL STUDY; MICROSATELLITE MARKER; MULTIPLE SCLEROSIS; PRIORITY JOURNAL; SIBLING; STATISTICAL ANALYSIS; STATISTICAL SIGNIFICANCE;

CANADA; CHROMOSOMES, HUMAN, PAIR 6; GENE FREQUENCY; GENES, MHC CLASS II; GENETIC MARKERS; GENETIC SCREENING; GENOME, HUMAN; HUMANS; LINKAGE DISEQUILIBRIUM; MICROSATELLITE REPEATS; MULTIPLE SCLEROSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; POPULATION; SIBLINGS;

EID: 2542547323     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/ddh123     Document Type: Article

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