Browsing by Subject Heterozygote

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PreviewIssue DateTitleAuthor(s)AdvisorType
2008Absence Of Mutations In Pax6 Gene In Three Cases Of Morning Glory Syndrome Associated With Isolated Growth Hormone Deficiency.Guerra-Junior, Gil; Spinola-Castro, Angela Maria; Siviero-Miachon, Adriana A; Nogueira, Roberto Gomes; Lemos-Marini, Sofia Helena V; D'Souza-Li, Lilia Freire Rodrigues; Silva, Priscila Cristina da; França, Emerson Salvador S; Soardi, Fernanda Caroline; Mello, Maricilda Palandi de-Artigo de periódico
2008Heterozygosis For Cyp21a2 Mutation Considered As 21-hydroxylase Deficiency In Neonatal Screening.Soardi, Fernanda Caroline; Lemos-Marini, Sofia Helena V; Coeli, Fernanda Borchers; Maturana, Víctor Gonçalves; Silva, Márcia Duarte Barbosa da; Bernardi, Renan Darin; Justo, Giselle Zenker; de-Mello, Maricilda Palandi-Artigo de periódico
2004Interleukin 10 Gene Promoter Polymorphisms Are Associated With Chronic Periodontitis.Scarel-Caminaga, Raquel M; Trevilatto, Paula C; Souza, Ana P; Brito, Rui B; Camargo, Luis E A; Line, Sergio R P-Artigo de periódico
2011Novel Human Crygd Rare Variant In A Brazilian Family With Congenital Cataract.de Figueirêdo, Eugênio Santana; Giordano, Gabriel Gorgone; Tavares, Anderson; da Silva, Márcio José; de Vasconcellos, José Paulo Cabral; Arieta, Carlos Eduardo Leite; de Melo, Mônica Barbosa-Artigo de periódico
2011Characterization Of Microsatellite Loci In Himatanthus Drasticus (apocynaceae), A Medicinal Plant From The Brazilian Savanna.Baldauf, Cristina; Ciampi, Maísa B; Vigna, Bianca B Z; Mori, Gustavo M; Guedes, Julian P P; De Souza, Anete P; Dos Santos, Flavio A M-Artigo de periódico
2001Hydroxyurea Promotes The Reduction Of Spontaneous Bfu-e To Normal Levels In Ss And S/beta Thalassemic Patients.Bincoletto, C; Perlingeiro, R C; Saad, S T; Costa, F F; Queiroz, M L-Artigo de periódico
-Mild Hemolysis In A Girl With G6pd Sumaré (class I Variant) Associated With G6pd A-.Saad, Sara T O; Costa, Fernando F-Artigo de periódico
2003Thalassemia Intermedia As A Result Of Heterozygosis For Beta 0 -thalassemia And Alpha Alpha Alpha Anti-3,7 Genotype In A Brazilian Patient.Kimura, E M; Grignoli, C R E; Pinheiro, V R P; Costa, F F; Sonati, M F-Artigo de periódico
2006Reticulocyte Evaluation In Alpha(+)-thalassemia.Krügner, F; Zaccariotto, T R; Rosim, E T; Costa, F F; Grotto, H Z W; Sonati, M F-Artigo de periódico
2007The Relationship Between Abo Groups And Subgroups, Factor Viii And Von Willebrand Factor.Sousa, Norma Cristina; Anicchino-Bizzacchi, Joyce Maria; Locatelli, Maria Fátima; Castro, Vagner; Barjas-Castro, Maria Lourdes-Artigo de periódico
2004Hb Osu-christiansborg [beta52(d3)asp --> Asn]: A De Novo Mutation In Brazil.Rodrigues de Souza, Laudicéia; Kimura, Elza Miyuki; Albuquerque, Dulcinéia Martins; Costa, Fernando Ferreira; de Fátima Sonati, Maria-Artigo de periódico
-Molecular Investigation In Children Candidates And Submitted To Cochlear Implantation.Bernardes, Raquel; Bortoncello, Silvana; Christiani, Thalita Vitachi; Sartorato, Edi Lúcia; Silva, Rodrigo César e; Porto, Paulo R Cantanhede-Artigo de periódico
2011Development And Characterization Of Microsatellite Markers For Hebanthe Eriantha (amaranthaceae).Figueira, Glyn M; Bajay, Miklos Maximiliano; Silva, Carolina M S; Zucchi, Maria I; Monteiro, Mariza; Rodrigues, Marili V N-Artigo de periódico
2009Microsatellite Markers For Population Genetic Studies Of The Blowfly Chrysomya Putoria (diptera: Calliphoridae).Rodrigues, Rosangela Aparecida; de Azeredo-Espin, Ana Maria Lima; Torres, Tatiana Teixeira-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
1992The 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 Patient.Costa, F F; Figueredo, M S; Sonati, M F; Kimura, E M; Martins, C S-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
1998Prothrombin Mutant, Factor V Leiden, And Thermolabile Variant Of Methylenetetrahydrofolate Reductase Among Patients With Sickle Cell Disease In Brazil.Andrade, F L; Annichino-Bizzacchi, J M; Saad, S T; Costa, F F; Arruda, V R-Artigo de periódico
1999New Frameshift Mutation In The 5alpha-reductase Type 2 Gene In A Brazilian Patient With 5alpha-reductase Deficiency.Ferraz, L F; Mathias Baptista, M T; Maciel-Guerra, A T; Júnior, G G; Hackel, C-Artigo de periódico
201246,xx Dsd And Antley-bixler Syndrome Due To Novel Mutations In The Cytochrome P450 Oxidoreductase Gene.Guaragna-Filho, Guilherme; Castro, Carla Cristina Telles de Sousa; Carvalho, Rodrigo Ribeiro De; Coeli, Fernanda Borchers; Ferraz, Lúcio Fábio Caldas; Petroli, Reginaldo José; Mello, Maricilda Palandi De; Sewaybricker, Letícia Esposito; Lemos-Marini, Sofia Helena Valente; D'Souza-Li, Lilia Freire Rodrigues; Miranda, Márcio Lopes; Maciel-Guerra, Andréa Trevas; Guerra-Junior, Gil-Artigo de periódico