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- 2019
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Mark
Targeted re-sequencing of F8, F9 and VWF : Characterization of Ion Torrent data and clinical implications for mutation screening
(
- Contribution to journal › Article
- 2018
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Mark
Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients
(
- Contribution to journal › Article
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Mark
Genetic Variation in the Syntaxin-Binding Protein STXBP5 in Type 1 von Willebrand Disease Patients
(
- 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
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Mark
Chronic rhinosinusitis patients show accumulation of genetic variants in PARS2
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- Contribution to journal › Article
- 2014
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Mark
Replication study of genetic variants associated with chronic rhinosinusitis and nasal polyposis
(
- Contribution to journal › Letter
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Mark
Genetic Variation in KLK2 and KLK3 Is Associated with Concentrations of hK2 and PSA in Serum and Seminal Plasma in Young Men
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- Contribution to journal › Article
- 2013
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Mark
Copy number variants in the kallikrein gene cluster.
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- Contribution to journal › Article
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Mark
Investigating highly replicated asthma genes as candidate genes for allergic rhinitis
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- Contribution to journal › Article
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Mark
Poor Reproducibility of Allergic Rhinitis SNP Associations
(
- Contribution to journal › Article