Paediatric Haematology Research Unit
231 – 240 of 269
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=""
width=""
height=""
allowtransparency="true"
frameborder="0">
</iframe>
- 1992
-
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
-
Mark
Implantable central venous catheter facilitates prophylactic treatment in children with haemophilia
- Contribution to journal › Article
-
Mark
Origin of mutation in sporadic cases of haemophilia-B
- Contribution to journal › Article
- 1991
-
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
Population genetics of the Malmö polymorphism of coagulation factor IX
- 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
A new strategy for carrier and prenatal diagnosis and molecular studies in haemophilia B
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
- 1990
-
Mark
Hepatitis C virus transmission by monoclonal antibody purified factor VIII concentrate
- Contribution to journal › Letter
