Molecular pathology of haemophilia B von Green, P. M., Bentley, D. R., Mibashan, R. S., Nilsson, I. M., Giannelli, F.

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FETAL HAEMOGLOBIN MEASUREMENT IN THE ASSESSMENT OF RED CELL ISOIMMUNISATION von Nicolaides, K.H., Clewell, W.H., Mibashan, R.S., Soothill, P.W., Rodeck, C.H., Campbell, S.

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Cordocentesis in the investigation of fetal erythropoiesis von Nicolaides, K.H., Thilaganathan, B., Mibashan, R.S.

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Have Liley charts outlived their usefulness? von Nicolaides, K.H., Rodeck, C.H., Mibashan, R.S., Kemp, J.R.

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Erythroblastosis and reticulocytosis in anemic fetuses von Nicolaides, K.H., Thilaganathan, B., Rodeck, C.H., Mibashan, R.S.

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Effect of the choice of WHO International Reference Preparation for thromboplastin on International Normalised Ratios von Poller, L, Taberner, D A, Thomson, J M, Morris, J, Mibashan, R S, Shinton, N K

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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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Human Embryonic ζ-Globin Chains in Fetal and Newborn Blood von Chui, David H.K., Mentzer, William C., Patterson, Margaret, Iarocci, Terri A., Embury, Stephen H., Perrine, Susan P., Mibashan, Reuben S., Higgs, Douglas R.

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A factor IX mutation, verified by direct genomic sequencing, causes haemophilia B by a novel mechanism von Tsang, T. C., Bentley, D. R., Mibashan, R. S., Giannelli, F.

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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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Fetoscopy in the assessment of unexplained fetal hydrops von NICOLAIDES, K. H., RODECK, C. H., LANGE, I., WATSON, J., GOSDEN, C. M., MILLER, D., MIBASHAN, R. S., MONIZ, C., MORGAN‐CAPNER, P., CAMPBELL, S.

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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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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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Normal blood cell values in the early mid-trimester fetus von Millar, D. S., Davis, L. R., Rodeck, C. H., Nicolaides, K. H., Mibashan, R. S.

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Guidelines on oral anticoagulation: second edition von DAVIDSON, J. F, COLVIN, B. T, BARROWCLIFFE, T. W, KERNOFF, P. B. A, MACHIN, S. J, POLLER, L, PRESTON, F. E, WALKER, I. D, MIBASHAN, R. S, SHINTON, N. K

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Selective feticide of the affected twin by fetoscopic air embolism von Rodeck, C. H., Mibashan, R. S., Abramowicz, J., Campbell, S.

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First-trimester diagnosis of Wiskott-Aldrich syndrome by DNA markers von SCHWARTZ, M, MIBASHAN, R. S, NICOLAIDES, K. H, MILLAR, D. S, JENKINS, E, RODECK, C. H, ØRSTAVIK, K. H, STORMORKEN, H

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Prenatal diagnosis of haemoglobinopathies by ion exchange hplc of haemoglobins von Rouyer-Fessard, P., Plassa, F., Blouquit, Y., Vidaud, M., Varnavides, L., Mibashan, R. S., Bellingham, A., Beuzard, Y.

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First trimester prenatal diagnosis and detection of carriers of haemophilia A using the linked DNA probe DX13 von Winter, R M, Harper, K, Goldman, E, Mibashan, R S, Warren, R C, Rodeck, C H, Penketh, R J, Ward, R H, Hardisty, R M, Pembrey, M E

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Prenatal diagnosis of β thalassaemia by reverse phase HPLC von Rouyer-Fessard, Ph, Beuzard, Y., Vidaud, M., John, P., Mibashan, R. S.

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