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British Journal of Haematology|December 3, 1999
Specific analysis of the intron 22 XbaI polymorphism of the human factor VIII gene using long-distance PCRC D De Brasi, D J Bowen, P W Collins, et al.
Journal of Thrombosis and Haemostasis : JTH|February 21, 2008
Developing a new generation of tests for genotyping hemophilia-causative rearrangements involving int22h and int1h hotspots in the factor VIII geneL C Rossetti, C P Radic, I B Larripa, et al.
Sangre|December 1, 1989
[Bloom syndrome, constitutional and induced genetic instability in 2 cases from Argentina]N B Gorla, M M Bonduel, H Lejarraga, et al.
Human Genetics|July 1, 1992
Increased expression of 5q31 fragile site in a Bloom syndrome familyA F Fundia, N B Gorla, M M Bonduel, et al.
Clinical Genetics|February 1, 1994
Chromosome instability in lymphocytes from patients with celiac diseaseA F Fundia, M B González Cid, J Bai, et al.
Leukemia & Lymphoma|August 28, 1998
Promyelocytic blast crisis of chronic myelogenous leukaemia with translocations (9;22) and (15;17)M P Scolnik, M F Palacios, S H Acevedo, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 29, 2013
Factor VIII genotype characterization of haemophilia A affected patients with transient and permanent inhibitors: a comprehensive Argentine study of inhibitor risksL C Rossetti, I Szurkalo, C P Radic, et al.
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