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PreviewIssue DateTitleAuthor(s)AdvisorType
2005Molecular Analysis Of Kal-1, Gnrh-r, Nelf And Ebf2 Genes In A Series Of Kallmann Syndrome And Normosmic Hypogonadotropic Hypogonadism Patients.Trarbach, Ericka B; Baptista, Maria T M; Garmes, Heraldo M; Hackel, Christine-Artigo de periódico
2001Antithrombin Deficiency In Brazilian Patients With Venous Thrombosis: Molecular Characterization Of A Single Splice Site Mutation, An Insertion And A De Novo Point Mutation.Arnaldi, L A; Pretti, F A; Zampieri, J P; Ramos, C F; Arruda, V R; Annichino-Bizzacchi, J M-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
2011Searching For Digenic Inheritance In Deaf Brazilian Individuals Using The Multiplex Ligation-dependent Probe Amplification Technique.da Silva-Costa, Sueli M; Martins, Fábio Tadeu Arrojo; Pereira, Tânia; Pomilio, Mariza C A; Marques-de-Faria, Antonia Paula; Sartorato, Edi Lúcia-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
2003Prevalence Of Factor Vii Deficiency And Molecular Characterization Of The F7 Gene In Brazilian Patients.Rodrigues, Dalva N; Siqueira, Lucia H; Galizoni, Andréa M; Arruda, Valder R; Annichino-Bizzacchi, Joyce M-Artigo de periódico
2004Weakened Expression Of 'e' Owing To Concomitant Occurrence Of Cys16 And Val245 (vs Antigen).Rodrigues, A; Rios, M; Costa, F F; Saad, S T O; Pellegrino, J; Castilho, L-Artigo de periódico
2003Genotyping Of Human Cytomegalovirus Using Non-radioactive Single-strand Conformation Polymorphism (sscp) Analysis.de Albuquerque, Dulcinéia Martins; Costa, Sandra Cecília Botelho-Artigo de periódico
2003Beta-thalassemia Intermedia In A Brazilian Patient With-101 (c > T) And Codon 39 (c > T) Mutations.de Sousa, Sylvia Morais; Khater, Letícia; Peroni, Luis Antônio; Miranda, Karine; Murai, Marcelo Jun; Albuquerque, Dulcinéia Marlins; Arruda, Paulo; Saad, Sara Terezinha Ollala; Costa, Fernando Ferreira-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
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
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
-1-Uns- -1Molecular Characterization Of Glucose-6-phosphate Dehydrogenase Deficiency In Brazil.Saad, S T; Salles, T S; Carvalho, M H; Costa, F F-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
1998Mutations Of Androgen Receptor Gene In Brazilian Patients With Male Pseudohermaphroditism.Cabral, D F; Maciel-Guerra, A T; Hackel, C-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
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
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