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Hematological Oncology|September 24, 2004
High sensitivity of chemiluminescent methodology for detection of clonal CDR3 sequences in patients with acute lymphoblastic leukemiaE Leal, A R Jaloma-Cruz, P Barros-NúñezHaemophilia : the Official Journal of the World Federation of Hemophilia|July 14, 2005
Thrombin generation and phenotypic correlation in haemophilia AC P Beltrán-Miranda, A Khan, A R Jaloma-Cruz, et al.Human Mutation|September 12, 2000
Novel hotspot detector software reveals a non-CpG hotspot of germline mutation in the factor IX gene (F9) in Latin AmericansJ B Drost, W A Scaringe, A R Jaloma-Cruz, et al.Archives of Medical Research|June 8, 2001
Y-chromosome haplotypes for six short tandem repeats (STRs) in a Mexican populationH Rangel-Villalobos, A R Jaloma-Cruz, L Sandoval-Ramírez, et al.International Journal of Laboratory Hematology|September 6, 2008
Kinetics of factor VIII:C inhibitors and treatment response in severe hemophilia A patientsH Luna-Záizar, M A Esparza-Flores, B López-Guido, et al.Hematological Oncology|February 28, 2003
Detection and monitoring of clonality in peripheral blood and bone marrow of patients with B-cell lymphoproliferative disordersE Leal, M A Esparza-Flores, B López-Guido, et al.Forensic Science International|December 22, 1999
Allele frequency distributions of six Amp-FLPS (D1S80, APO-B, VWA, TH01, CSF1PO and HPRTB) in a Mexican populationH Rangel-Villalobos, F Rivas, M Torres-Rodríguez, et al.Genetics and Molecular Research : GMR|November 4, 2016
Molecular thrombophilic profile in Mexican patients with idiopathic recurrent pregnancy lossJ J López-Jiménez, Á Porras-Dorantes, C I Juárez-Vázquez, et al.Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion|January 25, 2002
[The genetic DNA trace in men: chromosome Y haplotypes in a Mexican population, analyzing 5 STRs]H Rangel-Villalobos, A R Jaloma-Cruz, L Cerda-Aguilar, et al.Human Mutation|December 29, 1999
Nine independent F9 mutations in the Mexican hemophilia B population: nonrandom recurrences of point mutation events in the human germlineA R Jaloma-Cruz, W A Scaringe, J B Drost, et al.Pageof 2