Browsing by Subject Gene Frequency

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PreviewIssue DateTitleAuthor(s)AdvisorType
2008Polymorphisms Of Methylenetetrahydrofolate Reductase (mthfr), Methionine Synthase (mtr), Methionine Synthase Reductase (mtrr), And Thymidylate Synthase (tyms) In Multiple Myeloma Risk.Lima, Carmen S P; Ortega, Manoela M; Ozelo, Margareth C; Araujo, Renato C; De Souza, Cármino A; Lorand-Metze, Irene; Annichino-Bizzacchi, Joyce M; Costa, Fernando F-Artigo de periódico
-Genetic Variation And Relationships At Six Vntr Loci In Two Distinct Sample Populations In Brazil.Ramos, C F; Magna, L A; de Mello, M P; Silva, R; de Moura-Neto, R S-Artigo de periódico
2004Hyperhomocysteinemia And Mthfr C677t And A1298c Polymorphisms Are Associated With Chronic Allograft Nephropathy In Renal Transplant Recipients.Pavarino-Bertelli, E C; Sanches de Alvarenga, M P; Goloni-Bertollo, E M; Baptista, M A S F; Haddad, R; Hoerh, N F; Eberlin, M N; Abbud-Filho, M-Artigo de periódico
2014Rh, Kell, Duffy, Kidd And Diego Blood Group System Polymorphism In Brazilian Japanese Descendants.Flôres, Marli Aparecida Luvisuto Rossett; Visentainer, Jeane Eliete Laguila; Guelsin, Gláucia Andréia Soares; Fracasso, Adriana de Souza; de Melo, Fabiano Cavalcante; Hashimoto, Margareth Naomi; Sell, Ana Maria-Artigo de periódico
2010Vkorc1 V66m Mutation In African Brazilian Patients Resistant To Oral Anticoagulant Therapy.Orsi, Fernanda A; Annichino Bizzacchi, Joyce M; de Paula, Erich V; Ozelo, Margareth C; Langley, Michael R; Weck, Karen E-Artigo de periódico
2007Polymorphism C776g In The Transcobalamin Ii Gene And Homocysteine, Folate And Vitamin B12 Concentrations. Association With Mthfr C677t And A1298c And Mtrr A66g Polymorphisms In Healthy Children.Aléssio, Ana C M; Höehr, Nelci F; Siqueira, Lúcia H; Bydlowski, Sérgio P; Annichino-Bizzacchi, Joyce M-Artigo de periódico
2007Molecular Genetics Study Of Deafness In Brazil: 8-year Experience.de Oliveira, Camila Andréa; Alexandrino, Fabiana; Christiani, Thalita Vitachi; Steiner, Carlos Eduardo; Cunha, José Luiz Rosemberis; Guerra, Andréa Trevas Maciel; Sartorato, Edi Lúcia-Artigo de periódico
-Haptoglobin Polymorphism And Diabetic Nephropathy In Brazilian Diabetic Patients.Wobeto, Vânia P A; Garcia, Priscila M D; Zaccariotto, Tânia R; Sonati, Maria de Fátima-Artigo de periódico
2009Complex Patterns Of Genetic Variability In Populations Of The New World Screwworm Fly Revealed By Mitochondrial Dna Markers.Lyra, M L; Klaczko, L B; Azeredo-Espin, A M L-Artigo de periódico
2014Apoliprotein E Genotype Is Associated With Apoliprotein B Plasma Levels But Not With Coronary Calcium Score In Very Elderly Individuals In Primary Care Setting.Henriques, Adriane D; Tonet-Furioso, Audrey C; Machado-Silva, Wilcelly; Freitas, Wladimir M; Quaglia, Luiz A; Santos, Simone N; Córdova, Cláudio; Sposito, Andrei C; Nóbrega, Otávio T-Artigo de periódico
1994Two Dinucleotide Repeats Tightly Linked To D12s91.de Souza, A P; Allamand, V; Richard, I; Brenguier, L; Beckmann, J S-Artigo de periódico
1994Three Dinucleotide Markers On Chromosome 21.de Souza, A P; Allamand, V; Richard, I; Brenguier, L; Beckmann, J S-Artigo de periódico
2014Patients With Systemic Sclerosis Present Increased Dna Damage Differentially Associated With Dna Repair Gene Polymorphisms.Palomino, Gustavo Martelli; Bassi, Carmen L; Wastowski, Isabela J; Xavier, Danilo J; Lucisano-Valim, Yara M; Crispim, Janaina C O; Rassi, Diane M; Marques-Neto, Joao F; Sakamoto-Hojo, Elza T; Moreau, Philippe; Sampaio-Barros, Percival D; Donadi, Eduardo A-Artigo de periódico
2013Hla Markers For Poor Prognosis In Systemic Sclerosis Brazilian Patients.Del Rio, Ana Paula Toledo; Sachetto, Zoraida; Sampaio-Barros, Percival Degrava; Marques-Neto, João Francisco; Londe, Ana Carolina Santos; Bertolo, Manoel Barros-Artigo de periódico
1995Factor V Leiden (fvq 506) Is Common In A Brazilian Population.Arruda, V R; Annichino-Bizzacchi, J M; Costa, F F; Reitsma, P H-Artigo de periódico
1991High Prevalence Of Alpha-thalassemia In A Black Population Of Brazil.Sonati, M F; Farah, S B; Ramalho, A S; Costa, F F-Artigo de periódico
2013Polymorphism In The Hmox1 Gene Is Associated With High Levels Of Fetal Hemoglobin In Brazilian Patients With Sickle Cell Anemia.Gil, Gislene P; Ananina, Galina; Oliveira, Mariana B; Costa, Fernando F; Silva, Márcio J; Santos, Magnun N N; Bezerra, Marcos A C; Hatzlhofer, Betânia L D; Araujo, Aderson S; Melo, Mônica B-Artigo de periódico
1992Glucose-6-phosphate Dehydrogenase Deficiency And Sickle Cell Disease In Brazil.Saad, S T; Costa, F F-Artigo de periódico
1996Molecular Analysis Of Cyp21 And C4 Genes In Brazilian Families With The Classical Form Of Steroid 21-hydroxylase Deficiency.de-Araujo, M; Sanches, M R; Suzuki, L A; Guerra, G; Farah, S B; de-Mello, M P-Artigo de periódico
1996Hereditary Hemoglobinopathies In A Population From Southeast Brazil.Sonati, M F; Kimura, E M; Grotto, H Z; Gervasio, S A; Costa, F F-Artigo de periódico