Elsy Sjörin (Former)
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- 2012
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Mark
Investigation of disease-associated factors in haemophilia A patients without detectable mutations.
(
- Contribution to journal › Article
- 2010
-
Mark
Hemophilia A patients without detectable mutations - investigation of disease-associated factors
(
- Contribution to journal › Published meeting abstract
- 2008
-
Mark
Female haemophilia A caused by skewed X inactivation
(
- Contribution to journal › Letter
-
Mark
Why does the mutation G17736A/Val107Val (silent) in the F9 gene cause mild haemophilia B in five Swedish families?
(
- Contribution to journal › Article
- 2006
-
Mark
Functional Analysis of the Factor IX Epidermal Growth Factor-Like Domain Mutation Ile66Thr Associated with Mild Hemophilia B.
(
- Contribution to journal › Article
- 2003
-
Mark
Functional analysis of the EGF-like domain mutations Pro55Ser and Pro55Leu, which cause mild hemophilia B.
(
- Contribution to journal › Article
- 2002
-
Mark
Inhibitors in the Swedish population with severe haemophilia A and B : A 20-year survey
(
- Contribution to journal › Article
- 2001
-
Mark
Haemophilia B mutations in Sweden: a population-based study of mutational heterogeneity
(
- Contribution to journal › Article
- 1999
-
Mark
Origin of mutation in sporadic cases of haemophilia A
(
- Contribution to journal › Article
- 1995
-
Mark
Inversions of the factor VIII gene in Swedish patients with severe haemophilia A
(
- 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