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Methods in Molecular Medicine|February 23, 2011
Use of Intron 40 VNTR I in vWD Gene TrackingM S Enayat, G K SurdharThrombosis and Haemostasis|October 6, 2000
A new candidate missense mutation (Leu 1657 IIe) in an apparently asymptomatic type 2A (phenotype IIA) von Willebrand disease familyM S Enayat, A M Guilliatt, G K Surdhar, et al.Blood|July 27, 2001
Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of 3 different families with type 2A (phenotype IID) von Willebrand diseaseM S Enayat, A M Guilliatt, G K Surdhar, et al.Pageof 1