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	1.	A new candidate missense mutation (Leu 1657 IIe) in an apparently asymptomatic type 2A (phenotype IIA) von Willebrand disease family. [electronic resource] by Enayat, M S Guilliatt, A M Surdhar, G K Theophilus, B D Hill, F G Producer: 20010329 In: Thrombosis and haemostasis vol. 84 Availability: No items available. Save to lists Add to cart (remove)
	2.	Deletions and duplications in the factor VIII gene identified using multiplex ligation-dependent probe amplification. [electronic resource] by Theophilus, B D M Baugh, L M Guilliatt, A M Motwani, J Williams, M D Producer: 20110621 In: Journal of thrombosis and haemostasis : JTH vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Characterisation of type 2N von Willebrand disease using phenotypic and molecular techniques. [electronic resource] by Nesbitt, I M Goodeve, A C Guilliatt, A M Makris, M Preston, F E Peake, I R Producer: 19970325 In: Thrombosis and haemostasis vol. 75 Availability: No items available. Save to lists Add to cart (remove)
	4.	Novel characterization of a breakpoint in F8: an individualized approach to gene analysis when PCR and MLPA results contradict. [electronic resource] by Pezeshkpoor, B Theophilus, B D M Guilliatt, A M Oldenburg, J Williams, M D El-Maarri, O Producer: 20160118 In: Haemophilia : the official journal of the World Federation of Hemophilia vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A novel alanine or threonine 789 to proline mutation causing type 2N von Willebrand's disease when inherited homozygously or heterozygously with arginine 854 to glutamine mutation. [electronic resource] by Enayat, M S Guilliatt, A M Short, P E Rastegar-Lari, G Jazebi, M Ravonbod, S Ala, F Chapman, O G Hill, F G H Producer: 20110224 In: Haemophilia : the official journal of the World Federation of Hemophilia vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	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 disease. [electronic resource] by Enayat, M S Guilliatt, A M Surdhar, G K Jenkins, P V Pasi, K J Toh, C H Williams, M D Hill, F G Producer: 20010913 In: Blood vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)