Browsing by Subject Gene Deletion

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PreviewIssue DateTitleAuthor(s)AdvisorType
-A Naturally Occurring Deletion In The Sry Promoter Region Affecting The Sp1 Binding Site Is Associated With Sex Reversal.Assumpção, J G; Ferraz, L F Caldas; Benedetti, C E; Maciel-Guerra, A T; Guerra, G; Marques-de-Faria, A P; Baptista, M T Matias; de Mello, M P-Artigo de periódico
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
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
-Abo Blood Group In Amerindians From Brazilian Amazon.Barjas-Castro, M L; Soares, M C P; Menezes, R C; Carvalho, M H M; Costa, F F; Saad, S T O-Artigo de periódico
2002Alpha-thalassemia Does Not Significantly Contribute To The Low Mcv Level Of Hb C Trait.Silva, Nadia M; Soledade, Cinira S; Costa, Fernando F; Sonati, Maria F-Artigo de periódico
2002Hemoglobin H Disease Resulting From The Association Of The - Alpha 3.7 Rightward Deletion And The (alpha Alpha)mm Deletion In A Brazilian Patient.Wenning, M R S C; Harteveld, C L; Giordano, P C; Kimura, E M; Saad, S T O; Costa, F F; Sonati, M F-Artigo de periódico
2001High Prevalence Of Alpha-thalassemia Among Individuals With Microcytosis And Hypochromia Without Anemia.Borges, E; Wenning, M R; Kimura, E M; Gervásio, S A; Costa, F F; Sonati, M F-Artigo de periódico
2011Genomic Imbalances Detected Through Array Cgh In Fetuses With Holoprosencephaly.Machado, Isabela Nelly; Heinrich, Juliana Karina; Barini, Ricardo-Artigo de periódico
2003The Hansenula Polymorpha Mox Gene Presents Two Alternative Transcription Start Points Differentially Utilized And Sensitive To Respiratory Activity.Genu, Victor; Gödecke, Stefanie; Hollenberg, Cornelis P; Pereira, Gonçalo G-Artigo de periódico
2006Yeast Oxidative Stress Response. Influences Of Cytosolic Thioredoxin Peroxidase I And Of The Mitochondrial Functional State.Demasi, Ana P D; Pereira, Gonçalo A G; Netto, Luis E S-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
2010Novel Deletion Alleles Carrying Cyp21a1p/a2 Chimeric Genes In Brazilian Patients With 21-hydroxylase Deficiency.Coeli, Fernanda B; Soardi, Fernanda C; Bernardi, Renan D; de Araújo, Marcela; Paulino, Luciana C; Lau, Ivy F; Petroli, Reginaldo J; de Lemos-Marini, Sofia H V; Baptista, Maria T M; Guerra-Júnior, Gil; de-Mello, Maricilda P-Artigo de periódico
-[polymorphisms Gstm1 And Gstt1 And Sporadic Breast Cancer Mammographic Features].Morais, Lívia Martins Tavares Scianni; Cardoso Filho, Cássio; Lourenço, Gustavo Jacob; Shinzato, Julia Yoriko; Zeferino, Luiz Carlos; Lima, Carmen Sílvia Passos; Gurgel, Maria Salete Costa-Artigo de periódico
-Combination Of Angiotensin-converting Enzyme And Methylenetetrahydrofolate Reductase Gene Polymorphisms As Determinant Risk Factors For Chronic Allograft Dysfunction.de Alvarenga, M P S; Pavarino-Bertelli, E C; Abbud-Filho, M; Ferreira-Baptista, M A S; Haddad, R; Eberlin, M N; Goloni-Bertollo, E M-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
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
2013Study Of Candidate Genes For Dyslexia In Brazilian Individuals.Svidnicki, M C C M; Salgado, C A; Lima, R F; Ciasca, S M; Secolin, R; Pomilio, M C A; Junqueira, P A; Pinto, M S; Pereira, M M; Sartorato, E L-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
1999Mutation Distribution And Cyp21/c4 Locus Variability In Brazilian Families With The Classical Form Of The 21-hydroxylase Deficiency.Paulino, L C; Araujo, M; Guerra, G; Marini, S H; De Mello, M P-Artigo de periódico
2003Simple Fluorescent Pcr Method For Detection Of Large Deletions In The Beta-globin Gene Cluster.De Andrade, Tiago Gomes; Saad, Sara Teresinha Olalla; Sonati, Maria de Fatima; Costa, Fernando Ferreira-Artigo de periódico