Paediatric Hematologic Research Group
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- 1997
-
Mark
Identifying carriers at high risk for negative reactions when performing prenatal diagnosis of haemophilia
(
- Contribution to journal › Article
- 1996
-
Mark
Emergence of novel transient clonal chromosomal bone marrow changes in remission of acute lymphoblastic leukemia
(
- Contribution to journal › Article
- 1995
-
Mark
Inversions of the factor VIII gene in Swedish patients with severe haemophilia A
(
- Contribution to journal › Article
-
Mark
The impact of prenatal diagnosis on the incidence of haemophilia in Sweden
(
- Contribution to journal › Article
- 1992
-
Mark
Antenatal diagnosis of haemophilia B by amplification and electrophoresis of an exon fragment with a short deletion
(
- 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
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
- 1990
-
Mark
Hepatitis C virus transmission by monoclonal antibody purified factor VIII concentrate
(
- Contribution to journal › Letter