Annika Mårtensson
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- 2024
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Mark
Origin of pathogenic variant and mosaicism in families with a sporadic case of haemophilia B
(
- Contribution to journal › Article
- 2020
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Mark
Genetic screening of children with suspected inherited bleeding disorders
(
- Contribution to journal › Article
- 2016
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Mark
Origin of mutation in sporadic cases of severe haemophilia A in Sweden.
(
- Contribution to journal › Article
- 2015
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Mark
Haemophilia in Sweden – Studies on mutations and clinical implications
(
- Thesis › Doctoral thesis (compilation)
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Mark
Mutation analysis of Swedish haemophilia B families - high frequency of unique mutations.
2015) In Haemophilia(
- Contribution to journal › Article
- 2014
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Mark
Prenatal diagnosis of haemophilia in Sweden now more commonly used for psychological preparation than termination of pregnancy.
(
- Contribution to journal › Article
- 2013
-
Mark
Origin of Swedish hemophilia B mutations
(
- Contribution to journal › Article
- 2011
-
Mark
Thirty-years' experience of prenatal diagnosis of haemophilia in Sweden
2011) XXIII Congress of the International Society on Thrombosis and Haemostasis In Journal of Thrombosis and Haemostasis 9. p.462-462(
- Contribution to journal › Published meeting abstract