Molecular analysis of the WNT4 gene in 6 patients with Mayer-Rokitansky-Küster-Hauser syndrome von Drummond, Juliana B., M.D., M.Sc, Reis, Fernando M., M.D., Ph.D, Boson, Wolfanga L.M., M.D., M.Sc, Silveira, Leticia F.G., M.D., M.Sc, Bicalho, Maria A.C., M.D., M.Sc, De Marco, Luiz, M.D., Ph.D

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Novel mutations of the BSCL2 and AGPAT2 genes in 10 families with Berardinelli-Seip congenital generalized lipodystrophy syndrome von Miranda, Debora M., Wajchenberg, Bernardo L., Calsolari, Maria R., Aguiar, Marcos J., Silva, José M. C. L., Ribeiro, Marcia G., Fonseca, Cristina, Amaral, Daniela, Boson, Wolfanga L., Resende, Bruna A., De Marco, Luiz

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A Novel Mutation of the Cathepsin C Gene in Papillon‐Lefévre Syndrome von Cury, Vanessa F., Costa, José E., Gomez, Ricardo S., Boson, Wolfanga L., Loures, Cyro G., De Marco, Luiz

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A signal peptide mutation of the arginine vasopressin gene in monozygotic twins von Boson, Wolfanga L., Sarubi, Juliana C., D’Alva, Catarina B., Friedman, Eitan, Faria, Daniela, De Marco, Luiz, Wajchenberg, Bernardo

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Nephrogenic Diabetes Insipidus (NDI): Clinical, Laboratory and Genetic Characterization of Five Brazilian Patients von Vaisbich, Maria Helena, Carneiro, Juliana, Bóson, Wolfanga, Resende, Bruna, De Marco, Luiz, Honjo, Rachel S, Kim, Chong Ae, Koch, Vera H

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A Novel Mutation of the Cathepsin C Gene in Papillon-Lefévre Syndrome von Cury, Vanessa F, Costa, José E, Gomez, Ricardo S, Boson, Wolfanga L, Loures, Cyro G, De Marco, Luiz

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Association study of T102C 5-HT2A polymorphism in schizophrenic patients: diagnosis, psychopathology, and suicidal behavior von Correa, Humberto, De Marco, Luiz, Boson, Wolfanga, Nicolato, Rodrigo, Teixeira, Antó L., Campo, Valdir R., Romano-Silva, Marco A.

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Association study of T102C 5-HT(2A) polymorphism in schizophrenic patients: diagnosis, psychopathology, and suicidal behavior von Correa, Humberto, De Marco, Luiz, Boson, Wolfanga, Nicolato, Rodrigo, Teixeira, António L, Campo, Valdir R, Romano-Silva, Marco A

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Association study of T102C 5-HT 2A polymorphism in schizophrenic patients: diagnosis, psychopathology, and suicidal behavior von Correa, Humberto, De Marco, Luiz, Boson, Wolfanga, Nicolato, Rodrigo, Teixeira, Antó L., Campo, Valdir R., Romano-Silva, Marco A.

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Microsatellite Instability in Sporadic Parathyroid Adenoma 1 von Sarquis, Marta, Friedman, Eitan, Boson, Wolfanga L., Gomez, Ricardo S., Dias, Adalberto F., De Marco, Luiz

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Microsatellite Instability in Sporadic Parathyroid Adenoma1 von Sarquis, Marta, Friedman, Eitan, Boson, Wolfanga L., Gomez, Ricardo S., Dias, Adalberto F., De Marco, Luiz

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Microsatellite instability in sporadic parathyroid adenoma von Sarquis, M, Friedman, E, Boson, W L, Gomez, R S, Dias, A F, De Marco, L

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Mutational Analyses of Candidate Genes in Human Squamous Cell Carcinomas von Petroianu, Andy, Boson, Wolfanga L., Bale, Allen E., Friedman, Eitan, De Marco, Luiz

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Molecular analyses of the vasopressin type 2 receptor and aquaporin-2 genes in Brazilian kindreds with nephrogenic diabetes insipidus von Rocha, Juliane L., Friedman, Eitan, Boson, Wolfanga, Moreira, Ayrton, Figueiredo, Bonald, Liberman, Bernardo, de Lacerda, Luiz, Sandrini, Romulo, Graf, Hans, Martins, Sonia, Puñales, Marcia K., De Marco, Luiz

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Nephrogenic diabetes insipidus: An X chromosome-linked dominant inheritance pattern with a vasopressin type 2 receptor gene that is structually normal von Friedman, Eitan, Bale, Allen E, Carson, Emma, Boson, Wolfanga L

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Sporadic cardiac myxomas and tumors from patients with Carney complex are not associated with activating mutations of the Gsα gene von DEMARCO, L, STRATAKIS, C. A, FRIEDMAN, E, BOSON, W. L, JAKBOVITZ, O, CARSON, E, ANDRADE, L. M, AMARAL, V. F, ROCHA, J. L, CHOURSOS, G. P, NORDENSKJÖLD, M

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Nephrogenic Diabetes Insipidus: An X Chromosome-Linked Dominant Inheritance Pattern with a Vasopressin Type 2 Receptor Gene that is Structurally Normal von Friedman, Eitan, Bale, Allen E., Carson, Emma, Boson, Wolfanga L., Nordenskjöld, Magnus, Ritzén, Martin, Ferreira, Paulo C., Jammal, Anibal, De Marco, Luiz

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A signal peptide mutation of the arginine vasopressin gene in monozygotic twins von Boson, Wolfanga L., Sarubi, Juliana C., D'Alva, Catarina B., Friedman, Eitan, Faria, Daniela, De Marco, Luiz, Wajchenberg, Bernardo

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