FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high-risk group von ABU-DUHIER, F. M, GOODEVE, A. C, WILSON, G. A, GARI, M. A, PEAKE, I. R, REES, D. C, VANDENBERGHE, E. A, WINSHIP, P. R, REILLY, J. T

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Identification and functional characterization of a polymorphic oestrogen response element in the human coagulation factor IX gene promoter von Adams, B., Western, A. K., Winship, P. R.

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Key residues involved in calcium-binding motifs in EGF-like domains von Handford, P. A, Mayhew, M, Baron, M, Winship, P. R, Campbell, I. D, Brownlee, G. G

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A rapid method for haemophilia B mutation detection using conformation sensitive gel electrophoresis von Hinks, J. L., Winship, P. R., Makris, M., Preston, F. E., Peake, I. R., Goodeve, A. C.

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Gene structure, expression profiling and mutation analysis of the tumour suppressor SHIP1 in Caucasian acute myeloid leukaemia von Gilby, D C, Goodeve, A C, Winship, P R, Valk, P J, Delwel, R, Reilly, J T

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Detection of polymorphisms at cytosine phosphoguanadine dinucleotides and diagnosis of haemophilia B carriers von WINSHIP, P. R, REES, D. J. G, ALKAN, M

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DETECTION OF POLYMORPHISMS AT CYTOSINE PHOSPHOGUANADINE DINUCLEOTIDES AND DIAGNOSIS OF HAEMOPHILIA B CARRIERS von Winship, P.R., Rees, D.J.G., Alkan, M.

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A less severe form of Haemophilia B Leyden von CROSSLEY, M, WINSHIP, P. R, AUSTEN, D. E. G, RIZZA, C. R, BROWNLEE, G. G

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A Gly → Ser Change Causes Defective Folding in Vitro of Calcium-binding Epidermal Growth Factor-like Domains from Factor IX and Fibrillin-1 von Whiteman, P, Downing, A K, Smallridge, R, Winship, P R, Handford, P A

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Protein engineering of the propeptide of human factor IX von Handford, P.A., Winship, P.R., Brownlee, G.G.

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The −1185 A/G and −1051 G/A dimorphisms in the von Willebrand factor gene promoter and risk of myocardial infarction von Di Bitondo, Rosa, Cameron, Cherie L., Daly, Martina E., Croft, Stuart A., Steeds, Rick P., Channer, Kevin S., Samani, Nilesh J., Lillicrap, David, Winship, Peter R.

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Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms von Winship, Peter R., Anson, Don S., Rizza, Charles R., Brownlee, George G.

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Haemophilia B caused by mutation of a potential thrombin cleavage site in factor IX von WINSHIP, P. R

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Oestrogenic repression of human coagulation factor VII expression mediated through an oestrogen response element sequence motif in the promoter region von Di Bitondo, Rosa, Hall, Adrian J., Peake, Ian R., Iacoviello, Licia, Winship, Peter R.

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An improved method for directly sequencing PCR amplified material using dimethyl sulphoxide von WINSHIP, P. R

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Nullisomic deletion of the mcf.2 transforming gene in two haemophilia B patients von Anson, D. S., Blake, D. J., Winship, P. R., Birnbaum, D., Brownlee, G. G.

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Identification of Different Gene Expression Patterns in Low and High Grade Non-Hodgkin's Lymphomas by Differential Display von Carter, Deborah, Goepel, John R., Winship, Peter R., Goyns, Malcolm H.

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CHARACTERISATION AND USE OF AN INTRAGENIC POLYMORPHIC MARKER FOR DETECTION OF CARRIERS OF HAEMOPHILIA B (FACTOR IX DEFICIENCY) von Giannelli, F, Choo, K.H, Winship, P.R, Rizza, C.R, Anson, D.S, G, D.J, Ferrari, N, Brownlee, G.G

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Gene therapy: myth or reality? Report of a conference von Winship, P R

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Prenatal diagnosis of haemophilia B carriers von Winship, PR

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