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Vox Sanguinis|January 1, 1990
Management of fetal alloimmune thrombocytopenia by weekly in utero platelet transfusionsM F Murphy, H W Pullon, P Metcalfe, et al.Human Genetics|August 1, 1990
Improved carrier detection of haemophilia A using novel RFLPs at the DXS115 (767) locusP Jedlicka, S Greer, D S Millar, et al.Blood|September 1, 1989
Human embryonic zeta-globin chains in fetal and newborn bloodD H Chui, W C Mentzer, M Patterson, et al.Human Genetics|December 1, 1990
The molecular genetic analysis of haemophilia A; characterization of six partial deletions in the factor VIII geneD S Millar, R A Steinbrecher, K Wieland, et al.British Journal of Obstetrics and Gynaecology|July 1, 1985
Fetoscopy in the assessment of unexplained fetal hydropsK H Nicolaides, C H Rodeck, I Lange, et al.Blood|December 1, 1990
The molecular genetic analysis of hemophilia A: a directed search strategy for the detection of point mutations in the human factor VIII geneJ K Pattinson, D S Millar, J H McVey, et al.British Medical Journal (Clinical Research Ed.)|September 21, 1985
First trimester prenatal diagnosis and detection of carriers of haemophilia A using the linked DNA probe DX13R M Winter, K Harper, E Goldman, et al.Pageof 3