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	21.	Characterization of the original Christmas disease mutation (cysteine 206----serine): from clinical recognition to molecular pathogenesis. [electronic resource] by Taylor, S A Duffin, J Cameron, C Teitel, J Garvey, B Lillicrap, D P Producer: 19920724 In: Thrombosis and haemostasis vol. 67 Availability: No items available. Save to lists Add to cart (remove)
	22.	Lymphoproliferative disease of "LAK cell" precursor large granular lymphocytes in association with celiac disease. [electronic resource] by Lopez, P Morris, D G Galbraith, P R Lillicrap, D P Pross, H F Producer: 19930831 In: American journal of hematology vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	What is a cure and how do we get there? [electronic resource] by Skinner, M W Lillicrap, D P McMillan, J Castro Ozelo, M Pierce, G F Producer: 20050419 In: Haemophilia : the official journal of the World Federation of Hemophilia vol. 10 Suppl 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Differential termination of primer extension: a novel, quantifiable method for detection of point mutations. [electronic resource] by Picketts, D J Cameron, C Taylor, S A Deugau, K V Lillicrap, D P Producer: 19920619 In: Human genetics vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Linked and intragenic probes for haemophilia A. [electronic resource] by Peake, I R Lillicrap, D P Liddell, M B Matthews, R J Bloom, A L Producer: 19851125 In: Lancet (London, England) vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	A mutation adjacent to the beta cleavage site of factor IX (valine 182 to leucine) results in mild haemophilia Bm. [electronic resource] by Taylor, S A Liddell, M B Peake, I R Bloom, A L Lillicrap, D P Producer: 19900830 In: British journal of haematology vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Comparison of phenotypic assessment and the use of two restriction fragment length polymorphisms in the diagnosis of the carrier state in haemophilia B. [electronic resource] by Lillicrap, D P Liddell, M B Matthews, R J Peake, I R Bloom, A L Producer: 19860502 In: British journal of haematology vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Cosegregation of von Willebrand factor gene polymorphisms and possible germinal mosaicism in type IIB von Willebrand disease. [electronic resource] by Murray, E W Giles, A R Bridge, P J Peake, I R Lillicrap, D P Producer: 19910506 In: Blood vol. 77 Availability: No items available. Save to lists Add to cart (remove)
	29.	A complete deletion of the factor IX gene and new TaqI variant in a hemophilia B kindred. [electronic resource] by Taylor, S A Lillicrap, D P Blanchette, V Giles, A R Holden, J J White, B N Producer: 19880914 In: Human genetics vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Factor IX Cardiff: a variant factor IX protein that shows abnormal activation is caused by an arginine to cysteine substitution at position 145. [electronic resource] by Liddell, M B Peake, I R Taylor, S A Lillicrap, D P Giddings, J C Bloom, A L Producer: 19891023 In: British journal of haematology vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Prevalence of factor V Leiden and activated protein C resistance in central retinal vein occlusion. [electronic resource] by Johnson, T M El-Defrawy, S Hodge, W G Leonard, B C Kertes, P J Lillicrap, D P Producer: 20010823 In: Retina (Philadelphia, Pa.) vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human gene. [electronic resource] by Koeberl, D D Bottema, C D Ketterling, R P Bridge, P J Lillicrap, D P Sommer, S S Producer: 19900904 In: American journal of human genetics vol. 47 Availability: No items available. Save to lists Add to cart (remove)
	33.	Absence of a bleeding tendency in severe acquired von Willebrand's disease. The role of platelet von Willebrand factor in maintaining normal hemostasis. [electronic resource] by Drouin, J Lillicrap, D P Izaguirre, C A Sutherland, M Windsor, S Benford, K Hoogendorn, H Giles, A R Producer: 19891107 In: American journal of clinical pathology vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	Variation of the non-factor VIII sequences detected by a probe from intron 22 of the factor VIII gene. [electronic resource] by Lillicrap, D P Taylor, S A Schuringa, P C Blanchette, V S Lovsted, J K Weiler, L J Bridge, P J Producer: 19900209 In: Blood vol. 75 Availability: No items available. Save to lists Add to cart (remove)
	35.	Recombination between the factor VIII gene and the DXS52 locus gives the most probable genetic order as centromere-fra(X)-DXS15-DXS52-F8C-telomere. [electronic resource] by Mulligan, L M Grover, H J Blanchette, V S Giles, A R Lillicrap, D P Phillips, A Holden, J J White, B N Producer: 19870514 In: American journal of medical genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	Haemophilia B: database of point mutations and short additions and deletions--third edition, 1992. [electronic resource] by Giannelli, F Green, P M High, K A Sommer, S Lillicrap, D P Ludwig, M Olek, K Reitsma, P H Goossens, M Yoshioka, A Producer: 19920706 In: Nucleic acids research vol. 20 Suppl Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	Haemophilia B: database of point mutations and short additions and deletions--second edition. [electronic resource] by Giannelli, F Green, P M High, K A Sommer, S Lillicrap, D P Ludwig, M Olek, K Reitsma, P H Goossens, M Yoshioka, A Producer: 19910710 In: Nucleic acids research vol. 19 Suppl Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Haemophilia B: database of point mutations and short additions and deletions, fifth edition, 1994. [electronic resource] by Giannelli, F Green, P M Sommer, S S Lillicrap, D P Ludwig, M Schwaab, R Reitsma, P H Goossens, M Yoshioka, A Brownlee, G G Producer: 19941108 In: Nucleic acids research vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	Haemophilia B: database of point mutations and short additions and deletions. [electronic resource] by Giannelli, F Green, P M High, K A Lozier, J N Lillicrap, D P Ludwig, M Olek, K Reitsma, P H Goossens, M Yoshioka, A Producer: 19900906 In: Nucleic acids research vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	Report of a joint WHO/WFH meeting on the control of haemophilia: carrier detection and prenatal diagnosis. [electronic resource] by Peake, I R Lillicrap, D P Boulyjenkov, V Briët, E Chan, V Ginter, E K Kraus, E M Ljung, R Mannucci, P M Nicolaides, K Producer: 19930629 In: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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