Haemophilia Inhibitor Genetics Study - Evaluation of a model for studies of complex diseases using linkage and association methods [5]

Haemophilia

Volumn 11, Issue 4, 2005, Pages 427-429

  Berntorp, Erik ^a   Astermark, J ^a   Donfield, S M ^b   Nelson, G W ^c   Oldenburg, J ^d   Shapiro, A D ^e   Dimichele, D M ^f   Ewenstein, B M ^g   Gomperts, Edward D ^g,h   Winkler, C A ^c  

^a LUND UNIVERSITY HOSPITAL   (Sweden)

^b RHO INC   (United States)

^c SAIC FREDERICK INC   (United States)

^d Institute of Transfusion Medicine and Immune Hematology   (Germany)

^e INDIANA HEMOPHILIA AND THROMBOSIS CENTER   (United States)

^f WEILL CORNELL MEDICAL COLLEGE   (United States)

^g BAXTER HEALTHCARE CORPORATION   (United States)

^h CHILDREN S HOSPITAL LOS ANGELES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 8;

ALLELE; GENE IDENTIFICATION; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC LINKAGE; GENETIC VARIABILITY; HEMOPHILIA; HLA TYPING; HUMAN; HUMAN GENOME; LETTER; MOLECULAR GENETICS; PHENOTYPE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

ALLELES; FAMILY HEALTH; GENOME, HUMAN; HEMOPHILIA A; HUMANS; LINKAGE DISEQUILIBRIUM;

EID: 22744433296     PISSN: 13518216     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1365-2516.2005.01119.x     Document Type: Letter

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