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Polymerase Chain Reaction amplification of two polymorphic simple repeat sequences within the von Willebrand factor gene: Application to family studies in von Willebrand disease
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Instability of repeats of the von Willebrand factor gene variable number tandem repeat sequence in intron 40
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Detection of engraftment and mixed chimerism following bone marrow transplantation using PCR amplification of a highly variable region - Variable number of tandem repeats (VNTR) in the von Willebrand factor gene
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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
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Characterisation of 98 alleles in 105 unrelated individuals in the F8VWF gene
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HLA-DR typing by PCR amplification sequence-specific primers (PCR-SSP) in 2 hours: An alternative to serological DR typing in clinical pratice including donor - Recipient matching in cadaveric transplants
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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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Peake, I.R., Bowen D.J., Bignell, P., Liddel, M.B., Sadler, J.E., Standen, G.R. & Bloom, A.L. (1990) 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. Blood, 76, 555-561.
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Allelic associations of two polymorphic microsatellites in intron 40 of the human von Willebrand factor gene
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Family studies in von Willebrand's disease by analysis of restriction fragment length polymorphisms and an intragenic variable number tandem repeat (VNTR) sequence
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Genetic variation in the Italian population at five tandem repeat loci amplified in vitro: Use in paternity testing
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