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The EMBO Journal|April 1, 1989
Molecular pathology of haemophilia BP M Green, D R Bentley, R S Mibashan, et al.Prenatal Diagnosis|November 1, 1985
Normal blood cell values in the early mid-trimester fetusD S Millar, L R Davis, C H Rodeck, et al.Journal of Clinical Pathology|January 1, 1993
Effect of the choice of WHO International Reference Preparation for thromboplastin on International Normalised RatiosL Poller, D A Taberner, J M Thomson, et al.Human Genetics|January 1, 1991
Molecular genetic analysis of factor X deficiency: gene deletion and germline mosaicismK Wieland, D S Millar, C B Grundy, et al.Lancet (London, England)|May 14, 1988
Fetal haemoglobin measurement in the assessment of red cell isoimmunisationK H Nicolaides, P W Soothill, W H Clewell, et al.Prenatal Diagnosis|January 1, 1989
Prenatal diagnosis of haemoglobinopathies by ion exchange HPLC of haemoglobinsP Rouyer-Fessard, F Plassa, Y Blouquit, et al.Transfusion Medicine (Oxford, England)|December 1, 1994
Antenatal management of fetomaternal alloimmune thrombocytopenia--report of 15 affected pregnanciesM F Murphy, A H Waters, H A Doughty, et al.Lancet (London, England)|June 23, 1979
Plasma assay of fetal factors VIIIC and IX for prenatal diagnosis of haemophiliaR S Mibashan, C H Rodeck, J K Thumpston, et al.British Journal of Haematology|April 1, 1986
Prenatal diagnosis of hereditary red cell membrane defectS A Morris, V Ohanian, M L Lewis, et al.Lancet (London, England)|November 8, 1980
Dual diagnosis of prenatal haemophilia A by measurement of fetal factor VIIIC and VIIIC antigen (VIIICAg)R S Mibashan, I R Peake, C H Rodeck, et al.Pageof 3