Browsing by Author de Mello, Maricilda P

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Showing results 1 to 7 of 7
PreviewIssue DateTitleAuthor(s)AdvisorType
2004Clinical Findings In Four Brazilian Families Affected By Saethre-chotzen Syndrome Without Twist Mutations.Nascimento, Sandra R D; de Mello, Maricilda P; Batista, Juliano C; Balarin, Marly A S; Lopes, Vera L Gil da Silva-Artigo de periódico
2009T Allele Of -344 C/t Polymorphism In Aldosterone Synthase Gene Is Not Associated With Resistant Hypertension.Lacchini, Riccardo; Sabha, Maricene; Coeli, Fernanda B; Favero, Fabrício F; Yugar-Toledo, Juan; Izidoro-Toledo, Tatiane C; Sandrim, Valéria C; Tanus-Santos, José E; de Mello, Maricilda P; Moreno, Heitor-Artigo de periódico
2002Differential Gene Expression In Response To Copper In Acidithiobacillus Ferrooxidans Analyzed By Rna Arbitrarily Primed Polymerase Chain Reaction.Paulino, Luciana Campos; de Mello, Maricilda P; Ottoboni, Laura M M-Artigo de periódico
2009Novel Mutations In Cyp11b1 Gene Leading To 11 Beta-hydroxylase Deficiency In Brazilian Patients.Soardi, Fernanda C; Penachioni, Junia Y; Justo, Giselle Z; Bachega, Tânia A S S; Inácio, Marlene; Mendonça, Berenice B; de Castro, Margaret; de Mello, Maricilda P-Artigo de periódico
2014Homozygous Inactivating Mutation In Nanos3 In Two Sisters With Primary Ovarian Insufficiency.Santos, Mariza G; Machado, Aline Z; Martins, Conceição N; Domenice, Sorahia; Costa, Elaine M F; Nishi, Mirian Y; Ferraz-de-Souza, Bruno; Jorge, Soraia A C; Pereira, Carlos A; Soardi, Fernanda C; de Mello, Maricilda P; Maciel-Guerra, Andrea T; Guerra-Junior, Gil; Mendonca, Berenice B-Artigo de periódico
2014Performance Of Phalangeal Quantitative Ultrasound Parameters In The Evaluation Of Reduced Bone Mineral Density Assessed By Dx In Patients With 21 Hydroxylase Deficiency.Gonçalves, Ezequiel M; Sewaybricker, Leticia E; Baptista, Fatima; Silva, Analiza M; Carvalho, Wellington R G; Santos, Allan O; de Mello, Maricilda P; Lemos-Marini, Sofia H V; Guerra, Gil-Artigo de periódico
2011A De Novo Cryptic 5p Deletion And 9p Duplication Detected By Subtelomeric Mlpa In A Boy With Cri Du Chat Syndrome.Lincoln-de-Carvalho, Carolina R; Vicente, Fabíola M P; Vieira, Társis A P; de Mello, Maricilda P; Marques-de-Faria, Antonia P-Artigo de periódico