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Results: 1-9 |
Results: 9
Site and type of mutations in the factor VIII gene in patients and carriers of haemophilia A
Authors: Theophilus, BDM Enayat, MS Williams, MD Hill, FGH
Citation: Bdm. Theophilus et al., Site and type of mutations in the factor VIII gene in patients and carriers of haemophilia A, HAEMOPHILIA, 7(4), 2001, pp. 381-391
Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of3 different families with type 2A (phenotype IID) von Willebrand disease
Authors: Enayat, MS Guilliatt, AM Surdhar, GK Jenkins, PV Pasi, KJ Toh, CH Williams, MD Hill, FGH
Citation: Ms. Enayat et al., Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of3 different families with type 2A (phenotype IID) von Willebrand disease, BLOOD, 98(3), 2001, pp. 674-680
Homozygous gene conversion in von Willebrand factor gene as a cause of type 3 von Willebrand disease and predisposition to inhibitor development
Authors: Surdhar, GK Enayat, MS Lawson, S Williams, MD Hill, FGH
Citation: Gk. Surdhar et al., Homozygous gene conversion in von Willebrand factor gene as a cause of type 3 von Willebrand disease and predisposition to inhibitor development, BLOOD, 98(1), 2001, pp. 248-250
Identification of type 2 von Willebrand disease in previously diagnosed type 1 patients. a reappraisal using phenotypes, genotypes and molecular modelling
Authors: Nitu-Whalley, IC Riddell, A Lee, CA Pasi, KJ Owens, D Enayat, MS Perkins, SJ Jenkins, PV
Citation: Ic. Nitu-whalley et al., Identification of type 2 von Willebrand disease in previously diagnosed type 1 patients. a reappraisal using phenotypes, genotypes and molecular modelling, THROMB HAEM, 84(6), 2000, pp. 998-1004
A new candidate missense mutation (Leu 1657 IIe) in an apparently asymptomatic type 2A (phenotype IIA) von Willebrand disease family
Authors: Enayat, MS Guilliatt, AM Surdhar, GK Theopilus, BDM Hill, FGH
Citation: Ms. Enayat et al., A new candidate missense mutation (Leu 1657 IIe) in an apparently asymptomatic type 2A (phenotype IIA) von Willebrand disease family, THROMB HAEM, 84(3), 2000, pp. 369-373
Restriction fragment length polymorphism
Authors: Enayat, MS
Citation: Ms. Enayat, Restriction fragment length polymorphism, NUCLEIC ACID PROTOCOLS HANDBOOK, 2000, pp. 679-684
Congenital thrombophilia and thrombosis: a study in a single centre
Authors: Lawson, SE Butler, D Enayat, MS Williams, MD
Citation: Se. Lawson et al., Congenital thrombophilia and thrombosis: a study in a single centre, ARCH DIS CH, 81(2), 1999, pp. 176-178
Use of intron 40 VNTR I in vWD gene tracking
Authors: Enayat, MS Surdhar, GK
Citation: Ms. Enayat et Gk. Surdhar, Use of intron 40 VNTR I in vWD gene tracking, METH MOL M, 31, 1999, pp. 179-186
Multimeric analysis of von Willebrand Factor
Authors: Enayat, MS
Citation: Ms. Enayat, Multimeric analysis of von Willebrand Factor, METH MOL M, 31, 1999, pp. 187-200
Risultati: 1-9 |