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- 2020
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Mark
Genetic screening of children with suspected inherited bleeding disorders
(
- Contribution to journal › Article
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Mark
A rare heterozygous variant in FGB (Fibrinogen Merivale) causing hypofibrinogenemia in a Swedish family
(
- Contribution to journal › Article
- 2019
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Mark
A simplified flow cytometric method for detection of inherited platelet disorders—A comparison to the gold standard light transmission aggregometry
(
- Contribution to journal › Article
- 2018
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Mark
Germline heterozygous variants in genes associated with familial hemophagocytic lymphohistiocytosis as a cause of increased bleeding
(
- Contribution to journal › Article
- 2017
-
Mark
Application of whole-exome sequencing to direct the specific functional testing and diagnosis of rare inherited bleeding disorders in patients from the Öresund Region, Scandinavia
(
- Contribution to journal › Article