Diagnosing von Willebrand disease: genetic analysis.

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Diagnosing von Willebrand disease: genetic analysis.

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2016 nî lūn-bûn

@nan

2016年の論文

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2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

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2016年论文

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2016年论文

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Diagnosing von Willebrand disease: genetic analysis.

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Diagnosing von Willebrand disease: genetic analysis.

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Diagnosing von Willebrand disease: genetic analysis.

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Diagnosing von Willebrand disease: genetic analysis.

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Diagnosing von Willebrand disease: genetic analysis.

@en

Diagnosing von Willebrand disease: genetic analysis.

@nl

P1476

Diagnosing von Willebrand disease: genetic analysis.

@en

P2093

Anne Goodeve

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P2860

Critical von Willebrand factor A1 domain residues influence type VI collagen binding.

Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: a cohort study of 67 patients.

von Willebrand factor: clinical features of inherited and acquired disorders.

Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium

Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor.

Functional characterization of a 13-bp deletion (c.-1522_-1510del13) in the promoter of the von Willebrand factor gene in type 1 von Willebrand disease.

The diagnosis and management of von Willebrand disease: a United Kingdom Haemophilia Centre Doctors Organization guideline approved by the British Committee for Standards in Haematology.

Crucial role for the VWF A1 domain in binding to type IV collagen.

A Laboratory Phenotype/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease: A New Epidemiologic Picture.

von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA).

P304

678-682

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scholarly article

P356

10.1182/ASHEDUCATION-2016.1.678

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2016

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2016-12-01T00:00:00Z

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27913546

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6065508

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