Haplotype tagging for the identification of common disease genes

Nature Genetics

Volumn 29, Issue 2, 2001, Pages 233-237

  Johnson, Gillian C L ^a   Esposito, Laura ^a   Barratt, Bryan J ^a   Smith, Annabel N ^a   Heward, Joanne ^b   Di Genova, Gianfranco ^a   Ueda, Hironori ^a   Cordell, Heather J ^a   Eaves, Iain A ^a   Dudbridge, Frank ^a   Twells, Rebecca C J ^a   Payne, Felicity ^a   Hughes, Wil ^a   Nutland, Sarah ^a   Stevens, Helen ^a   Carr, Phillipa ^a   Tuomilehto Wolf, Eva ^c   Tuomilehto, Jaakko ^c,d   Gough, Stephen C L ^b   Clayton, David G ^a   Todd, John A ^a   more..

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b UNIVERSITY DEPARTMENT OF MEDICINE   (United Kingdom)

^c NATIONAL PUBLIC HEALTH INSTITUTE   (Finland)

^d UNIVERSITY OF HELSINKI   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

NUCLEOTIDE;

ARTICLE; CALCULATION; DNA DETERMINATION; GENE ISOLATION; GENE LINKAGE DISEQUILIBRIUM; GENE MAPPING; GENETIC LINKAGE; GENOTYPE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

BASE SEQUENCE; DNA; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE HOMOLOGY, NUCLEIC ACID;

EID: 0034789532     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng1001-233     Document Type: Article

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