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F F Costa

Showing results (91-100 of 228) with videos related to

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British Journal of Haematology|June 1, 1997
Beta-spectrin Campinas: a novel shortened beta-chain variant associated with skipping of exon 30 and hereditary elliptocytosisD S Basserès, P H Pranke, T S Sales, et al.
British Journal of Haematology|February 13, 2001
A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosisP G Gallagher, J D Ferreira, F F Costa, et al.
Journal of Medical Genetics|September 1, 1993
Molecular characterisation of beta thalassaemia heterozygotes in BrazilC S Martins, A S Ramalho, M F Sonati, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|September 3, 2005
Hemochromatosis (HFE) gene mutations in Brazilian chronic hemodialysis patientsF V Perícole, M A V R Alves, S T O Saad, et al.
British Journal of Haematology|October 1, 1994
Red cell membrane protein abnormalities in hereditary spherocytosis in BrazilS T Saad, F F Costa, D L Vicentim, et al.
Sao Paulo Medical Journal = Revista Paulista De Medicina|September 1, 1996
Comparison of red cell distribution width and a red cell discriminant function incorporating volume dispersion for distinguishing iron deficiency from beta thalassemia trait in patients with microcytosisC S Lima, A R Reis, H Z Grotto, et al.
Acta Haematologica|March 22, 2000
Molecular characterization of hemoglobins Kurosaki [alpha7 Lys-->Glu], G-Pest [alpha74 Asp-->Asn], Stanleyville-II [alpha78 Asn-->Lys] and J-Rovigo [alpha53 Ala-->Asp]M R Wenning, E M Kimura, S B Jorge, et al.
Acta Ophthalmologica|October 1, 1990
Conjunctival vessel abnormalities in sickle cell diseases: the influence of age and genotypeW C Siqueira, M S Figueiredo, A A Cruz, et al.
Human Mutation|January 1, 1997
G6PD sumaré: a novel mutation in the G6PD gene (1292 T-->G) associated with chronic nonspherocytic anemiaS T Saad, T S Salles, V R Arruda, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|August 4, 2009
Influence of the polymorphisms of the alpha-major regulatory element HS-40 on in vitro gene expressionD M Ribeiro, T R Zaccariotto, M N N Santos, et al.
Pageof 23

Showing results (91-100 of 228) with videos related to

Sort By:
Pageof 23
British Journal of Haematology|June 1, 1997
Beta-spectrin Campinas: a novel shortened beta-chain variant associated with skipping of exon 30 and hereditary elliptocytosisD S Basserès, P H Pranke, T S Sales, et al.
British Journal of Haematology|February 13, 2001
A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosisP G Gallagher, J D Ferreira, F F Costa, et al.
Journal of Medical Genetics|September 1, 1993
Molecular characterisation of beta thalassaemia heterozygotes in BrazilC S Martins, A S Ramalho, M F Sonati, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|September 3, 2005
Hemochromatosis (HFE) gene mutations in Brazilian chronic hemodialysis patientsF V Perícole, M A V R Alves, S T O Saad, et al.
British Journal of Haematology|October 1, 1994
Red cell membrane protein abnormalities in hereditary spherocytosis in BrazilS T Saad, F F Costa, D L Vicentim, et al.
Sao Paulo Medical Journal = Revista Paulista De Medicina|September 1, 1996
Comparison of red cell distribution width and a red cell discriminant function incorporating volume dispersion for distinguishing iron deficiency from beta thalassemia trait in patients with microcytosisC S Lima, A R Reis, H Z Grotto, et al.
Acta Haematologica|March 22, 2000
Molecular characterization of hemoglobins Kurosaki [alpha7 Lys-->Glu], G-Pest [alpha74 Asp-->Asn], Stanleyville-II [alpha78 Asn-->Lys] and J-Rovigo [alpha53 Ala-->Asp]M R Wenning, E M Kimura, S B Jorge, et al.
Acta Ophthalmologica|October 1, 1990
Conjunctival vessel abnormalities in sickle cell diseases: the influence of age and genotypeW C Siqueira, M S Figueiredo, A A Cruz, et al.
Human Mutation|January 1, 1997
G6PD sumaré: a novel mutation in the G6PD gene (1292 T-->G) associated with chronic nonspherocytic anemiaS T Saad, T S Salles, V R Arruda, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|August 4, 2009
Influence of the polymorphisms of the alpha-major regulatory element HS-40 on in vitro gene expressionD M Ribeiro, T R Zaccariotto, M N N Santos, et al.
Pageof 23