Molecular testing for disorders of hemostasis. - Wikidata - wikimedia - TriplyDB

Molecular testing for disorders of hemostasis.

Molecular testing for disorders of hemostasis.

http://www.wikidata.org/entity/Q37602557

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Detection of mild inherited disorders of blood coagulation: current options and personal recommendations.Molecular Genetic Diagnosis of the Inherited Bleeding Disorders: Are We Close to the Perfect Test?

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Molecular testing for disorders of hemostasis.

http://www.wikidata.org/entity/Q37602557

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on June 2013

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Molecular testing for disorders of hemostasis.

@en

Molecular testing for disorders of hemostasis.

@nl

type

label

Molecular testing for disorders of hemostasis.

@en

Molecular testing for disorders of hemostasis.

@nl

prefLabel

Molecular testing for disorders of hemostasis.

@en

Molecular testing for disorders of hemostasis.

@nl

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International Journal of Laboratory Hematology

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Molecular testing for disorders of hemostasis.

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Isolation and characterization of a cDNA coding for human factor IX

Hundreds of variants clustered in genomic loci and biological pathways affect human height

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

The mutational spectrum of type 1 von Willebrand disease: Results from a Canadian cohort study.

The molecular basis of hemophilia A: genotype-phenotype relationships and inhibitor development.

VWF mutations and new sequence variations identified in healthy controls are more frequent in the African-American population.

Characteristics of inhibitors in mild/moderate haemophilia A.

Inhibitor development in haemophilia B: an orphan disease in need of attention.

Platelet-type von Willebrand disease and type 2B von Willebrand disease: a story of nonidentical twins when two different genetic abnormalities evolve into similar phenotypes.

Preimplantation genetic diagnosis of haemophilia.

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290-296

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scholarly article

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10.1111/IJLH.12078

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