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Results: 1-3 |
Results: 3
Heterozygosity for the H63D mutation in the hereditary hemochromatosis (HFE) gene may lead into severe iron overload in beta-thalassemia minor: Observations in a thalassemic kindred.
Authors: Ruiz-Arguelles, GJ Garces-Eisele, J Reyes-Nunez, V Sanchez-Anzaldo, J Ruiz-Delgado, GJ Jimenez-Gonzalez, C Carrera, B
Citation: Gj. Ruiz-arguelles et al., Heterozygosity for the H63D mutation in the hereditary hemochromatosis (HFE) gene may lead into severe iron overload in beta-thalassemia minor: Observations in a thalassemic kindred., REV INV CLI, 53(2), 2001, pp. 117-120
PML/RAR alpha(+) hypergranular acute promyelocytic leukemia (M3) developing into an M3 acute myelocytic leukemia without PML/RAR alpha
Authors: Ruiz-Arguelles, GJ Ruiz-Delgado, GJ Reyes-Nunez, V
Citation: Gj. Ruiz-arguelles et al., PML/RAR alpha(+) hypergranular acute promyelocytic leukemia (M3) developing into an M3 acute myelocytic leukemia without PML/RAR alpha, ACT HAEMAT, 104(2-3), 2000, pp. 124-127
The G20210A polymorphism in the 3 '-untranslated region of the prothrombingene in Mexican mestizo patients with primary antiphospholipid syndrome
Authors: Ruiz-Arguelles, GJ Garces-Eisele, J Ruiz-Delgado, GJ Alarcon-Segovia, D
Citation: Gj. Ruiz-arguelles et al., The G20210A polymorphism in the 3 '-untranslated region of the prothrombingene in Mexican mestizo patients with primary antiphospholipid syndrome, CL APPL T-H, 5(3), 1999, pp. 158-160
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