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Toxicology Letters|October 1, 1991
Lack of sensitivity of sister-chromatid exchange for lymphocyte chromosomal damage detection caused by antichagasic treatmentN B Gorla, O S Ledesma, G P Barbieri, et al.Mutation Research|October 1, 1989
Thirteenfold increase of chromosomal aberrations non-randomly distributed in chagasic children treated with nifurtimoxN B Gorla, O S Ledesma, G P Barbieri, et al.British Journal of Haematology|December 21, 2000
A new polymorphism in the human factor VIII gene: implications for linkage analysis in haemophilia A and for the evolution of int22h sequencesD J Bowen, C D De Brasi, I B Larripa, et al.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.Pageof 3