(Q45857734)

17 December 2017

title

Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian type 1 VWD study (English)

1 reference

17 December 2017

author

Andrew D. Paterson

2

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17 December 2017

author name string

P D James

1

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17 December 2017

C Notley

3

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17 December 2017

C Cameron

4

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17 December 2017

C Hegadorn

5

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17 December 2017

S Tinlin

6

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17 December 2017

C Brown

7

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17 December 2017

L O'Brien

8

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17 December 2017

J Leggo

9

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17 December 2017

D Lillicrap

10

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17 December 2017

ASSOCIATION OF HEMOPHILIA CLINIC DIRECTORS OF CANADA

11

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17 December 2017

publication date

1 April 2006

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17 December 2017

Journal of Thrombosis and Haemostasis

published in

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17 December 2017

volume

4

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17 December 2017

issue

4

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17 December 2017

page(s)

783-792

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17 December 2017

Molecular cloning of cDNA for human von Willebrand factor: authentication by a new method

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1 reference

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Sialyltransferase ST3Gal-IV operates as a dominant modifier of hemostasis by concealing asialoglycoprotein receptor ligands

21 January 2018

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Mvwf, a dominant modifier of murine von Willebrand factor, results from altered lineage-specific expression of a glycosyltransferase

21 January 2018

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Genetic determinants of hemostasis phenotypes in Spanish families.

21 January 2018

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Heritability of plasma concentrations of clotting factors and measures of a prethrombotic state in a protein C-deficient family

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2006.01860.X

Population differences in von Willebrand factor levels affect the diagnosis of von Willebrand disease in African-American women

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2006.01860.X

von Willebrand factor: clinical features of inherited and acquired disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2006.01860.X

Founder von Willebrand factor haplotype associated with type 1 von Willebrand disease

21 January 2018

1 reference

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Polymorphism and recombination events at the ABO locus: a major challenge for genomic ABO blood grouping strategies

21 January 2018

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Sequence variation at the human ABO locus.

21 January 2018

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The family based association test method: strategies for studying general genotype--phenotype associations.

21 January 2018

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PBAT: tools for family-based association studies

21 January 2018

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Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

21 January 2018

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Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patients

21 January 2018

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Type 1 von Willebrand disease mutation Cys1149Arg causes intracellular retention and degradation of heterodimers: a possible general mechanism for dominant mutations of oligomeric proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2006.01860.X

von Willebrand disease and quantitative variation in von Willebrand factor

21 January 2018

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New concepts in von Willebrand disease

21 January 2018

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Von Willebrand disease type 1: a diagnosis in search of a disease

21 January 2018

1 reference

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An association of candidate gene haplotypes and bleeding severity in von Willebrand disease (VWD) type 1 pedigrees

21 January 2018

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Prevalence of von Willebrand disease in children: a multiethnic study

21 January 2018

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Genetic studies in complex disease: the case pro linkage studies.

21 January 2018

1 reference

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The prevalence of the cysteine1584 variant of von Willebrand factor is increased in type 1 von Willebrand disease: co-segregation with increased susceptibility to ADAMTS13 proteolysis but not clinical phenotype.

21 January 2018

1 reference

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21 January 2018

Identifiers

DOI

1 reference

17 December 2017

1 reference

17 December 2017