Haemophilia B is caused by a heterogeneous spectrum of mutations. Mutation characterization is important in genetic counselling, prenatal diagnosis and to predict risk of inhibitor development
Heterogeneous mutations in factor IX (FIX) gene cause haemophilia B and a large number of mutation...
Haemophilia B is the third most common bleeding disorder, affecting 1:30000 males, caused by the def...
Hemophilia B (HB) is a disorder resulting from genetic mutations in the Factor 9 gene (F9). Genotypi...
The present series comprises all families (n = 77) with haemophilia B in Sweden and may be considere...
Introduction: Haemophilia A (HA) and B (HB) are two of our most common inherited bleeding disorders ...
Background More than 1100 mutations that cause hemophilia B (HB) have been identified. At the same t...
Hemophilia B is an X-chromosome-linked inherited bleeding disorder primarily affecting males, but th...
Carrier and prenatal diagnosis based on the identification of the gene defect (direct diagnosis) inc...
Hemophilia B (HB) is caused by mutations in the human gene F9. The mutation type plays a pivotal rol...
The nature of the mutation in the factor IX gene is an important factor in determining whether a pat...
The aim of this study was to ascertain how many of the sporadic cases of severe Haemophilia A in Swe...
Item does not contain fulltextHeterogeneous mutations in factor IX (FIX) gene cause haemophilia B an...
Hemophilia B (HB) is caused by mutations in the human gene F9. The muta-tion type plays a pivotal ro...
The aim of molecular genetic analysis in families with haemophilia is to identify the causative muta...
The aim of this study was to define the origin of mutation in sporadic cases of severe haemophilia A...
Heterogeneous mutations in factor IX (FIX) gene cause haemophilia B and a large number of mutation...
Haemophilia B is the third most common bleeding disorder, affecting 1:30000 males, caused by the def...
Hemophilia B (HB) is a disorder resulting from genetic mutations in the Factor 9 gene (F9). Genotypi...
The present series comprises all families (n = 77) with haemophilia B in Sweden and may be considere...
Introduction: Haemophilia A (HA) and B (HB) are two of our most common inherited bleeding disorders ...
Background More than 1100 mutations that cause hemophilia B (HB) have been identified. At the same t...
Hemophilia B is an X-chromosome-linked inherited bleeding disorder primarily affecting males, but th...
Carrier and prenatal diagnosis based on the identification of the gene defect (direct diagnosis) inc...
Hemophilia B (HB) is caused by mutations in the human gene F9. The mutation type plays a pivotal rol...
The nature of the mutation in the factor IX gene is an important factor in determining whether a pat...
The aim of this study was to ascertain how many of the sporadic cases of severe Haemophilia A in Swe...
Item does not contain fulltextHeterogeneous mutations in factor IX (FIX) gene cause haemophilia B an...
Hemophilia B (HB) is caused by mutations in the human gene F9. The muta-tion type plays a pivotal ro...
The aim of molecular genetic analysis in families with haemophilia is to identify the causative muta...
The aim of this study was to define the origin of mutation in sporadic cases of severe haemophilia A...
Heterogeneous mutations in factor IX (FIX) gene cause haemophilia B and a large number of mutation...
Haemophilia B is the third most common bleeding disorder, affecting 1:30000 males, caused by the def...
Hemophilia B (HB) is a disorder resulting from genetic mutations in the Factor 9 gene (F9). Genotypi...
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