A new polymorphism in the human factor VIII gene: Implications for linkage analysis in haemophilia A and for the evolution of int22h sequences

British Journal of Haematology

Volumn 111, Issue 2, 2000, Pages 544-548

  Fernández, Mireya ^a   Simon, Valeska ^a,b   Minguell, José J ^a,b  

^a UNIVERSITY OF CHILE   (Chile)

^b CLÍNICA LAS CONDES   (Chile)

Author keywords

Haemophilia A; int22h sequences; Intron 22; Linkage analysis; Polymorphism

Indexed keywords

BLOOD CLOTTING FACTOR 8;

ALLELE; ARTICLE; CAUCASIAN; CONTROLLED STUDY; GENE DUPLICATION; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCATION; GENE SEQUENCE; GENETIC LINKAGE; GENETIC POLYMORPHISM; HAPLOTYPE; HEMOPHILIA A; HUMAN; INTRON; MALE; MOLECULAR EVOLUTION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

CHROMOSOME MAPPING; EVOLUTION, MOLECULAR; FACTOR VIII; GENE FREQUENCY; GENOTYPE; HEMOPHILIA A; HETEROZYGOTE DETECTION; HUMANS; INTRONS; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; WALES;

EID: 0034532955     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2000.02373.x     Document Type: Article

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