Rolf Ljung
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- 1992
-
Mark
Gaucher's disease in an infant diagnosed by fine needle aspiration of the liver and spleen : A case report
- Contribution to journal › Article
-
Mark
Haplotype analysis of identical factor IX mutants using PCR
- Contribution to journal › Article
-
Mark
Further characterization of the new marker at DXS115 with regard to carrier detection in hemophilia A
- Contribution to journal › Letter
- 1991
-
Mark
A new strategy for carrier and prenatal diagnosis and molecular studies in haemophilia B
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
-
Mark
Moderate haemophilia B in a female carrier caused by preferential inactivation of the paternal X chromosome
- Contribution to journal › Article
-
Mark
More than half the sporadic cases of Hemophilia A in Sweden are due to a recent mutation
- Contribution to journal › Article
-
Mark
Haemophilia B mutations in a complete Swedish population sample : a test of new strategy for the genetic counselling of diseases with high mutational heterogeneity
- Contribution to journal › Article
-
Mark
Population genetics of the Malmö polymorphism of coagulation factor IX
- Contribution to journal › Article
- 1990
-
Mark
Hepatitis C virus transmission by monoclonal antibody purified factor VIII concentrate
- Contribution to journal › Letter
-
Mark
The incidence and distribution of CpG----TpG transitions in the coagulation factor IX gene. A fresh look at CpG mutational hotspots
- Contribution to journal › Article
