Late-onset homozygous protein C deficiency von Grundy, C.B, Melissari, E, Lindo, V, Scully, M.F, Kakkar, V.V, Cooper, D.N

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The Molecular Genetic Analysis of Hemophilia A: A Directed Search Strategy for the Detection of Point Mutations in the Human Factor VIII Gene von Pattinson, J.K., Millar, D.S., McVey, J.H., Grundy, C.B., Wieland, K., Mibashan, R.S., Martinowitz, U., Tan-Un, K., Vidaud, M., Goossens, M., Sampietro, M., Mannucci, P.M., Krawczak, M., Reiss, J., Zoll, B., Whitmore, D., Bowcock, S., Wensley, R., Ajani, A., Mitchell, V., Rizza, C., Maia, R., Winter, P., Mayne, E.E., Schwartz, M., Green, P.J., Kakkar, V.V., Tuddenham, E.G.D., Cooper, D.N.

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the molecular genetic analysis of haemophilia A ; characterization of six partial deletions in the factor VIII gene von MILLAR, D. S, STEINBRECHER, R. A, KAKKAR, V. V, COOPER, D. N, WIELAND, K, GRUNDY, C. B, MARTINOWITZ, U, KRAWCZAK, M, ZOLL, B, WHITMORE, D, STEPHENSON, J, MIBASHAN, R. S

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A novel homozygous missense mutation in the protein C (PROC) gene causing recurrent venous thrombosis von GRUNDY, C. B, CHISHOLM, M, KAKKAR, V. V, COOPER, D. N

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A novel nonsense mutation in the protein C (PROC) gene (Trp-29→Term) causing recurrent venous thrombosis von MILLAR, D. S, GRUNDY, C. B, BIGNELL, P, MITCHELL, D. C, CORDEN, D, WOODS, P, KAKKAR, V. V, COOPER, D. N

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Improved carrier detection of haemophilia A using novel RFLPs at the DXS115 (767) locus von JEDLICKA, P, GREER, S, MILLAR, D. S, GRUNDY, C. B, JENKINS, E, MITCHELL, M, MIBASHAN, R. S, KAKKAR, V. V, COOPER, D. N

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Protein C deficiency and thromboembolism: recurrent mutation at Arg 306 in the protein C gene von Grundy, C B, Schulman, S, Krawczak, M, Kobosko, J, Kakkar, V V, Cooper, D N

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A novel missense mutation in the antithrombin III gene (Ser349→Pro) causing recurrent venous thrombosis von GRUNDY, C. B, HOLDING, S, MILLAR, D. S, KAKKAR, V. V, COOPER, D. N

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Molecular genetic analysis of factor X deficiency : gene deletion and germline mosaicism von WIELAND, K, MILLAR, D. S, GRUNDY, C. B, MIBASHAN, R. S, KAKKAR, V. V, COOPER, D. N

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A Gla domain mutation (Arg 15→Trp) in the protein C (PROC) gene causing type 2 protein C deficiency and recurrent venous thrombosis von Millar, D S, Grundy, C B, Bignell, P, Moffat, E H, Martin, R, Kakkar, V V, Cooper, D N

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De novo splice site mutation in the antithrombin III (AT3) gene causing recurrent venous thrombosis: Demonstration of exon skipping by ectopic transcript analysis von Berg, Lutz-Peter, Grundy, Catherine B., Thomas, Frank, Millar, David S., Green, Peter J., Slomski, Ryszard, Reiss, Jochen, Kakkar, Vijay V., Cooper, David N.

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Two different missense mutations at Arg 178 of the protein C (PROC) gene causing recurrent venous thrombosis von GRUNDY, C. B, SCHULMAN, S, TENGBORN, L, KAKKAR, V. V, COOPER, D. N

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Recurrent Deletion in the Human Antithrombin III Gene von Grundy, Catherine B., Thomas, Frank, Millar, David S., Krawczak, Michael, Melissari, Euthemia, Lindo, Vivian, Moffat, Elizabeth, Kakkar, Vijay V., Cooper, David N.

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MspI RFLP in the human heparin cofactor II (HCF2) gene von Turner, J, Grundy, C B, Kakkar, V V, Cooper, D N

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Protein C deficiency and thrombomembolism : recurrent mutation at Arg 306 in the protein C gene von GRUNDY, C. B, SCHULMAN, S, KRAWCZAK, M, KOBOSKO, J, KAKKAR, V. V, COOPER, D. N

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Mspl RFLP in the human heparin cofactor II (HCF2) gene von TURNER, J, GRUNDY, C. B, KAKKAR, V. V, COOPER, D. N

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Ce qu'un Anglais trouve en France von Grundy, J B C

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Ce qu'un Anglais trouve en France von Grundy, J. B. C.

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Recurrent deletion in the human antirhombin III gene von GRUNDY, C. B, THOMAS, F, MILLAR, D. S, KRAWCZAK, M, MELISSARI, E, LINDO, V, MOFFAT, E, KAKKAR, V. V, COOPER, D. N

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HAZARDS OF SCOTTISH DANCING von Mcwilliam, P.M., Mcwilliam, L., Ireland, WilliamJ, Reinstein, JeromeA, Grundy, M., Grundy, C.B.

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