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PreviewIssue DateTitleAuthor(s)AdvisorType
2005Rhnull Syndrome: Identification Of A Novel Mutation In Rhce.Rosa, K A; Reid, M E; Lomas-Francis, C; Powell, V I; Costa, F F; Stinghen, S T; Watanabe, A M; Carboni, E K; Baldon, J P; Jucksch, M M F; Castilho, L-Artigo de periódico
2007Three Novel Mutations In The Activin Receptor-like Kinase 1 (alk-1) Gene In Hereditary Hemorrhagic Telangiectasia Type 2 In Brazilian Patients.Assis, A M; Costa, F F; Arruda, V R; Annichino-Bizzacchi, J M; Bertuzzo, C S-Artigo de periódico
2007Hb Indianapolis [beta112 (g14) Cys-->arg] As The Probable Cause Of Moderate Hemolytic Anemia And Renal Damage In A Brazilian Patient.Fattori, A; Kimura, E M; Albuquerque, D M; Oliveira, D M; Costa, F F; Sonati, M F-Artigo de periódico
2012Lack Of Association Between Mdm2 Snp309 And Tp53 Arg72pro Polymorphisms With Clinical Outcomes In Myelodysplastic Syndrome.Machado-Neto, J A; Traina, F; De Melo Campos, P; Andreoli-Risso, M F; Costa, F F; Olalla Saad, S T-Artigo de periódico
1998Molecular Analysis Of The Retinoblastoma (rb1) Gene In Acute Myeloid Leukemia Patients.Melo, M B; Costa, F F; Saad, S T; Lorand-Metze, I; Bordin, S; Ahmad, N N-Artigo de periódico
1999Spontaneous Erythroid Colony Formation In Brazilian Patients With Sickle Cell Disease.Perlingeiro, R C; Costa, F F; Saad, S T; Arruda, V R; Queiroz, M L-Artigo de periódico
1998Haplotype Analysis And Agamma Gene Polymorphism Associated With The Brazilian Type Of Hereditary Persistence Of Fetal Hemoglobin.Bordin, S; Martins, J T; Gonçalves, M S; Melo, M B; Saad, S T; Costa, F F-Artigo de periódico
1992Glucose-6-phosphate Dehydrogenase Deficiency And Sickle Cell Disease In Brazil.Saad, S T; Costa, F F-Artigo de periódico
-[differentiation Between Heterozygotic Beta-thalassemia And Iron Deficiency Anemia].Sonati, M de F; Grotto, H Z; Kimura, E M; Costa, F F-Artigo de periódico
-[detection Of Hemophilia A Gene Carriers In A Brazilian Population].Arruda, V R; Annichino-Bizzacchi, J M; Costa, F F-Artigo de periódico