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Instability of repeats of the von Willebrand factor gene variable number tandem repeat sequence in intron 40

Data up to Jan 2025

Published1993
Citations18
References13
Clinical Trials (1)

Total Citations Per Year

Abstract

References (13)

Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA

1988 • 773 citations

Structure of the gene for human von Willebrand factor

1989 • 497 citations

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

1990 • 160 citations

Unequal crossingover between homologous chromosomes is not the major mechanism involved in the generation of new alleles at VNTR loci

1989 • 147 citations

Isolation and mapping of a polymorphic DNA sequence pYNH24 on chromosome 2 (D2S44)

1987 • 100 citations

Tetranucleotide repeat polymorphism in the vWF gene

1990 • 76 citations

A Database of Polymorphisms in the von Willebrand Factor Gene and Pseudogene

1993 • 73 citations

Molecular characterization of a unique von Willebrand disease variant. A novel mutation affecting von Willebrand factor/factor VIII interaction

1991 • 66 citations

Intrinsic polymorphism of variable number tandem repeat loci in the human genome

1988 • 35 citations

Rsal polymorphism in von Willebrand factor (vWF) at codon 789

1990 • 23 citations

Characterisation of 98 alleles in 105 unrelated individuals in the F8VWF gene

1991 • 19 citations

An HphI‐polymorphism in exon 28 of the von Willebrand factor gene, and its frequency among patients with various forms of von Willebrand's disease

1991 • 16 citations

Von Willebrand disease family studies: comparison of three methods of analysis of the von Willebrand factor gene polymorphism related to a variable number tandem repeat sequence in intron 40

1992 • 8 citations

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