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F F Costa

Showing results (81-90 of 228) with videos related to

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Sangre|October 1, 1996
Rapid detection of factor V Leiden (FVQ506) by non-radioactive single strand conformation polymorphism (SSCP)V R Arruda, P M von Zuben, J M Annichino-Bizzachi, et al.
Vox Sanguinis|March 17, 2004
Weakened expression of 'e' owing to concomitant occurrence of Cys16 and Val245 (VS antigen)A Rodrigues, M Rios, F F Costa, et al.
American Journal of Hematology|May 20, 1999
Spontaneous erythroid colony formation in Brazilian patients with sickle cell diseaseR C Perlingeiro, F F Costa, S T Saad, et al.
Acta Haematologica|January 1, 1992
HbH disease associated with the (--MED) deletion in a Brazilian black womanM F Sonati, E M Kimura, H Z Grotto, et al.
Hemoglobin|January 1, 1992
The IVS-I-110 (G-->T) and codon 39 (C-->T) beta-thalassemia mutations in association with alpha-thal-2 (-3.7 Kb) and Hb Hasharon [alpha 47(CE5)Asp-->His] in a Brazilian patientF F Costa, M S Figueredo, M F Sonati, et al.
Blood|January 15, 1995
Glucose-6-phosphate dehydrogenase deficiency in sickle cell disease by DNA analysisS T Saad, F F Costa, T S Salles, et al.
Haematologia|September 5, 1998
The relationship of bone marrow histology with the molecular pattern in chronic myeloid leukemiaA C Vigorito, I Lorand-Metze, M L Chauffaile, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|October 1, 1993
Rapid identification of beta-globin structural mutations by sequencing the mRNA from peripheral blood reticulocytesS R Miranda, M S Gonçalves, M F Sonati, et al.
Hemoglobin|May 1, 1996
Hereditary hemoglobinopathies in a population from southeast BrazilM F Sonati, E M Kimura, H Z Grotto, et al.
Transfusion Medicine (Oxford, England)|February 17, 2005
High frequency of partial DIIIa and DAR alleles found in sickle cell disease patients suggests increased risk of alloimmunization to RhDL Castilho, M Rios, A Rodrigues, et al.
Pageof 23

Showing results (81-90 of 228) with videos related to

Sort By:
Pageof 23
Sangre|October 1, 1996
Rapid detection of factor V Leiden (FVQ506) by non-radioactive single strand conformation polymorphism (SSCP)V R Arruda, P M von Zuben, J M Annichino-Bizzachi, et al.
Vox Sanguinis|March 17, 2004
Weakened expression of 'e' owing to concomitant occurrence of Cys16 and Val245 (VS antigen)A Rodrigues, M Rios, F F Costa, et al.
American Journal of Hematology|May 20, 1999
Spontaneous erythroid colony formation in Brazilian patients with sickle cell diseaseR C Perlingeiro, F F Costa, S T Saad, et al.
Acta Haematologica|January 1, 1992
HbH disease associated with the (--MED) deletion in a Brazilian black womanM F Sonati, E M Kimura, H Z Grotto, et al.
Hemoglobin|January 1, 1992
The IVS-I-110 (G-->T) and codon 39 (C-->T) beta-thalassemia mutations in association with alpha-thal-2 (-3.7 Kb) and Hb Hasharon [alpha 47(CE5)Asp-->His] in a Brazilian patientF F Costa, M S Figueredo, M F Sonati, et al.
Blood|January 15, 1995
Glucose-6-phosphate dehydrogenase deficiency in sickle cell disease by DNA analysisS T Saad, F F Costa, T S Salles, et al.
Haematologia|September 5, 1998
The relationship of bone marrow histology with the molecular pattern in chronic myeloid leukemiaA C Vigorito, I Lorand-Metze, M L Chauffaile, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|October 1, 1993
Rapid identification of beta-globin structural mutations by sequencing the mRNA from peripheral blood reticulocytesS R Miranda, M S Gonçalves, M F Sonati, et al.
Hemoglobin|May 1, 1996
Hereditary hemoglobinopathies in a population from southeast BrazilM F Sonati, E M Kimura, H Z Grotto, et al.
Transfusion Medicine (Oxford, England)|February 17, 2005
High frequency of partial DIIIa and DAR alleles found in sickle cell disease patients suggests increased risk of alloimmunization to RhDL Castilho, M Rios, A Rodrigues, et al.
Pageof 23