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Human Molecular Genetics|July 1, 1994
Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cellsJ P Rossiter, M Young, M L Kimberland, et al.Blood|February 1, 1993
Human immunodeficiency virus-related conditions in children and adults with hemophilia: rates, relationship to CD4 counts, and predictive valueM E Eyster, C S Rabkin, M W Hilgartner, et al.Leukemia Research|January 1, 1996
Tissue factor expression in human leukemic cellsG A Hair, S Padula, R Zeff, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|February 17, 2000
Interaction of anti-phospholipid antibodies with late endosomes of human endothelial cellsB Galve-de Rochemonteix, T Kobayashi, C Rosnoblet, et al.Blood|July 13, 2000
Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemiaM Neerman-Arbez, P de Moerloose, C Bridel, et al.Thrombosis and Haemostasis|April 1, 1997
Clinical features in 36 patients homozygous for the ARG 506-->GLN factor V mutationJ Emmerich, M Alhenc-Gelas, M F Aillaud, et al.Human Genetics|May 17, 2001
Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genesM Neerman-Arbez, P de Moerloose, A Honsberger, et al.Haematologica|June 15, 2004
Analysis of biological phenotypes from 42 patients with inherited factor VII deficiency: can biological tests predict the bleeding risk?Muriel Giansily-Blaizot, Régis Verdier, Christine Biron-Adréani, et al.Blood|September 15, 1995
Factor VIII gene inversions in severe hemophilia A: results of an international consortium studyS E Antonarakis, J P Rossiter, M Young, et al.Pageof 21