Laboratory methods for the genetic diagnosis of bleeding disorders

Clinical and Laboratory Haematology

Volumn 20, Issue 1, 1998, Pages 3-19

  Goodeve, A C ^a  

^a ROYAL HALLAMSHIRE HOSPITAL   (United Kingdom)

Author keywords

Carrier analysis; Haemophilia; Mutation; Polymorphism; Von Willebrand's disease

Indexed keywords

BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 9; DNA; VON WILLEBRAND FACTOR;

BLEEDING DISORDER; CHROMOSOME XQ; GEL ELECTROPHORESIS; GENE AMPLIFICATION; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC POLYMORPHISM; HEMOPHILIA A; HEMOPHILIA B; HETEROZYGOTE DETECTION; HUMAN; LABORATORY TEST; POINT MUTATION; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; REVIEW; SOUTHERN BLOTTING; VON WILLEBRAND DISEASE;

GENETIC TECHNIQUES; HEMOPHILIA A; HEMOPHILIA B; HUMANS; METHODS; VON WILLEBRAND DISEASE;

EID: 0031915612     PISSN: 01419854     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2257.1998.00115.x     Document Type: Review

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