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PreviewIssue DateTitleAuthor(s)AdvisorType
2010The Novel Wt1 Gene Mutation P.h377n Associated To Denys-drash Syndrome.Guaragna, Mara Sanches; Soardi, Fernanda Caroline; Assumpção, Juliana Godoy; Zambaldi, Lílian de Jesus Girotto; Cardinalli, Izilda Aparecida; Yunes, José Andrés; de Mello, Maricilda Palandi; Brandalise, Silvia Regina; Aguiar, Simone dos Santos-Artigo de periódico
2013Optimization Of Simultaneous Screening Of The Main Mutations Involved In Non-syndromic Deafness Using The Taqman® Openarray™ Genotyping Platform.Martins, Fábio Tadeu Arrojo; Ramos, Priscila Zonzini; Svidnicki, Maria Carolina Costa Melo; Castilho, Arthur Menino; Sartorato, Edi Lúcia-Artigo de periódico
1995Eleven Novel Mutations In The Factor Viii Gene From Brazilian Hemophilia A Patients.Arruda, V R; Pieneman, W C; Reitsma, P H; Deutz-Terlouw, P P; Annichino-Bizzacchi, J M; Briët, E; Costa, F F-Artigo de periódico
1996Rapid Detection Of Factor V Leiden (fvq506) By Non-radioactive Single Strand Conformation Polymorphism (sscp).Arruda, V R; von Zuben, P M; Annichino-Bizzachi, J M; Costa, F F-Artigo de periódico
-Molecular Characterization Of Glucose-6-phosphate Dehydrogenase Deficiency In Brazil.Saad, S T; Salles, T S; Carvalho, M H; Costa, F F-Artigo de periódico
1998Mutations Of Androgen Receptor Gene In Brazilian Patients With Male Pseudohermaphroditism.Cabral, D F; Maciel-Guerra, A T; Hackel, C-Artigo de periódico
2012Thrombomodulin Is Required For The Antithrombotic Activity Of Thrombin Mutant W215a/e217a In A Mouse Model Of Arterial Thrombosis.Vicente, Cristina P; Weiler, Hartmut; Di Cera, Enrico; Tollefsen, Douglas M-Artigo de periódico
1997G6pd Sumaré: A Novel Mutation In The G6pd Gene (1292 T-->g) Associated With Chronic Nonspherocytic Anemia.Saad, S T; Salles, T S; Arruda, V R; Sonati, M F; Costa, F F-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
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
1997N-ras Gene Point Mutations In Brazilian Acute Myelogenous Leukemia Patients Correlate With A Poor Prognosis.De Melo, M B; Lorand-Metze, I; Lima, C S; Saad, S T; Costa, F F-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
1999Molecular Characterization Of Hemoglobins Kurosaki [alpha7 Lys-->glu], G-pest [alpha74 Asp-->asn], Stanleyville-ii [alpha78 Asn-->lys] And J-rovigo [alpha53 Ala-->asp].Wenning, M R; Kimura, E M; Jorge, S B; Costa, F F; Sonati, M F-Artigo de periódico
-Recurrence Of A Nonsense Mutation In The Conserved Domain Of Sry In A Brazilian Patient With 46,xy Gonadal Dysgenesis.Assumpção, J G; Guerra, A T; Palandi de Mello, M-Artigo de periódico
2000Molecular Heterogeneity Of The A3 Subgroup.Barjas-Castro, M L; Carvalho, M H; Locatelli, M F; Bordin, S; Saad, S T-Artigo de periódico
2003Phenotype And Genotype Correlation Of The Microconversion From The Cyp21a1p To The Cyp21a2 Gene In Congenital Adrenal Hyperplasia.Torres, N; Mello, M P; Germano, C M R; Elias, L L K; Moreira, A C; Castro, M-Artigo de periódico
2003Analysis Of The Mechanism Of Action Of The Brazilian Type (agamma-195 C --> G) Of Hereditary Persistence Of Fetal Hemoglobin.Takahashi, T; Schreiber, R; Krieger, J E; Saad, S T O; Costa, F F-Artigo de periódico
2003Screening For Mutations In Human Alpha-globin Genes By Nonradioactive Single-strand Conformation Polymorphism.Jorge, S B; Melo, M B; Costa, F F; Sonati, M F-Artigo de periódico
2004The Use Of Reverse Transcription-pcr For The Diagnosis Of X-linked Chronic Granulomatous Disease.Agudelo-Flórez, P; López, J A; Redher, J; Carneiro-Sampaio, M M S; Costa-Carvalho, B T; Grumach, A S; Condino-Neto, A-Artigo de periódico
2001The Agamma-195 (c-->g) Mutation In Hereditary Persistence Of Fetal Hemoglobin Is Not Associated With Activation Of A Reporter Gene In Vitro.Schreiber, R; Gonçalves, M S; Junqueira, M L; Saad, S T; Krieger, J E; Costa, F F-Artigo de periódico