Genetic heterogeneity of severe von Willebrand disease type III in the German population (Q42595743)

3 November 2017

Genetic heterogeneity of severe von Willebrand disease type III in the German population (English)

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3 November 2017

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R Schneppenheim

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S Krey

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F Bergmann

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D Bock

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U Budde

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M Lange

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R Linde

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U Mittler

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E Meili

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G Mertes

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1 December 1994

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94

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6

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640-652

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https://scigraph.springernature.com/pub.10.1007/bf00206958

3 November 2017

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cites work

A revised classification of von Willebrand disease. For the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.

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12 December 2020

A stop codon in a patient with severe type III von Willebrand disease

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12 December 2020

RsaI RFLP in the human von Willebrand factor gene

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12 December 2020

DNA methylation and the frequency of CpG in animal DNA.

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12 December 2020

A polymorphism of the human von Willebrand factor (vWf) gene with BamHI

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12 December 2020

Incidence of severe von Willebrand's disease

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12 December 2020

Delta C in exon 18 of the von Willebrand gene is uncommon in German vWD type III patients

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12 December 2020

A de novo and heterozygous gene deletion causing a variant of von Willebrand disease

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12 December 2020

Analysis of the VNTR locus D1S80 by the PCR followed by high-resolution PAGE

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12 December 2020

Family studies and prenatal diagnosis in severe von Willebrand disease by polymerase chain reaction amplification of a variable number tandem repeat region of the von Willebrand factor gene

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12 December 2020

An EcoRI polymorphism in the human von Willebrand factor (vWF) gene.

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12 December 2020

Enzyme-linked immunoabsorbent assay of factor VIII-related antigen. Interest in study of Von Willerbrand's disease (author's transl)

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12 December 2020

A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patients

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12 December 2020

Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization.

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12 December 2020

Mutations in severe, type III von Willebrand's disease in the Dutch population: candidate missense and nonsense mutations associated with reduced levels of von Willebrand factor messenger RNA

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12 December 2020

Gene deletions correlate with the development of alloantibodies in von Willebrand disease

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12 December 2020

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

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12 December 2020

Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene

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12 December 2020

Letter: A method for assaying von Willebrand factor (ristocetin cofactor)

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12 December 2020

The standardized normal Ivy bleeding time and its prolongation by aspirin

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12 December 2020

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

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12 December 2020

Two TaqI RFLPs in the human von Willebrand factor gene

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12 December 2020

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

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12 December 2020

The complex multimeric composition of factor VIII/von Willebrand factor

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12 December 2020

Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction

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12 December 2020

Atherosclerosis and von Willebrand factor. I. Prevalence of severe von Willebrand's disease in western Europe and Israel

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12 December 2020

Structure of the gene for human von Willebrand factor

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12 December 2020

Cloning and characterization of two cDNAs coding for human von Willebrand factor.

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12 December 2020

Genetic and blood coagulation characterization of "Swedish" families with von Willebrand's disease types I and III: new aspects of heredity

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12 December 2020

A computer program for selection of oligonucleotide primers for polymerase chain reactions

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12 December 2020

A second Xba I polymorphic site within the human von Willebrand factor (vWF) gene

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12 December 2020

Homozygous and heterozygous deletions of the von Willebrand factor gene in patients and carriers of severe von Willebrand disease

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12 December 2020

Severe type III von Willebrand's disease caused by deletion of exon 42 of the von Willebrand factor gene: family studies that identify carriers of the condition and a compound heterozygous individual

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12 December 2020

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12 December 2020

Construction of cDNA coding for human von Willebrand factor using antibody probes for colony-screening and mapping of the chromosomal gene.

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12 December 2020

The structure and function of von Willebrand factor

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12 December 2020

A polymorphic Xba I site within the human von Willebrand factor (vWF) gene identified by a vWF cDNA clone

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12 December 2020

SacI RFLP in the human von Willebrand factor gene

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12 December 2020

Frequency of different types of von Willebrand's disease in the GDR

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12 December 2020

Luminography--an alternative assay for detection of von Willebrand factor multimers

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12 December 2020

Differences between heterozygous dominant and recessive von Willebrand's disease type I expressed by bleeding symptoms and combinations of factor VIII variables

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12 December 2020

Molecular genetics of von Willebrand disease

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12 December 2020

Nonsense mutations of the von Willebrand factor gene in patients with von Willebrand disease type III and type I

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12 December 2020

Identifiers

DOI

10.1007/BF00206958

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Dimensions Publication ID

3 November 2017

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