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

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

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

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