Peripheral precocious puberty: 46, XY complete gonadal dysgenesis by Santalha, M, Amaral, B, Pereira, J, Ribeiro, L, João Oliveira, M, Figueiredo, S, Cardoso, H, Peixoto, C, Borges, T, Cidade-Rodrigues, J A

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P26.09: Prenatal diagnosis and management of a complex ovarian cyst: case report by Cerdeira, A. S., Marta, S., Ferreira, H. B., Taborda, F., Enes, C., Cidade‐Rodrigues, J. A., Macedo, R. Z.

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Swyer Syndrome and 46,XY Partial Gonadal Dysgenesis Associated with 9p Deletions in the Absence of Monosomy-9p Syndrome by Veitia, R.A., Nunes, M., Quintana-Murci, L., Rappaport, R., Thibaud, E., Jaubert, F., Fellous, M., McElreavey, K., Gonçalves, J., Silva, M., Cidade Rodrigues, J., Caspurro, M., Boieiro, F., Marques, R., Lavinha, J.

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CYP21A2 mutations in Portuguese patients with congenital adrenal hyperplasia: Identification of two novel mutations and characterization of four different partial gene conversions by Friães, Ana, Rêgo, Ana Toste, Aragüés, José Maria, Moura, Luís Francisco, Mirante, Alice, Mascarenhas, Mário Rui, Kay, Teresa Taylor, Lopes, Lurdes Afonso, Rodrigues, José Cidade, Guerra, Sílvia, Dias, Teresa, Teles, Alberto Galvão, Gonçalves, João

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17β-Hydroxysteroid dehydrogenase-3 deficiency: Diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de Novo mutations by BOEHMER, A. L. M, BRINKMANN, A. O, ROUWE, C. W, MENDONCA, B. B, RODRIGUES, C, BODE, H. H, DE RUITER, P. E, DE WAAL, H. A. D.-V, DROP, S. L. S, SANDKUIJL, L. A, HALLEY, D. J. J, NIERMEIJER, M. F, ANDERSSON, S, DE JONG, F. H, KAYSERILI, H, DE VROEDE, M. A, OTTEN, B. J

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Peripheral precocious puberty: 46,XY complete gonadal dysgenesis by Santalha, M., Amaral, B., Pereira, J., Ribeiro, L., João Oliveira, M., Figueiredo, S., Cardoso, H., Peixoto, C., Borges, T., Cidade-Rodrigues, J.A.

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Pubertad precoz periférica: disgenesia gonadal completa 46 XY by Santalha, M, Amaral, B, Pereira, J, Ribeiro, L, João Oliveira, M, Figueiredo, S, Cardoso, H, Peixoto, C, Borges, T, Cidade-Rodrigues, J.A

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17β-Hydroxysteroid Dehydrogenase-3 Deficiency: Diagnosis, Phenotypic Variability, Population Genetics, and Worldwide Distribution of Ancient and de Novo Mutations1 by Boehmer, Annemie L. M, Brinkmann, Albert O, Sandkuijl, Lodewijk A, Halley, Dicky J. J, Niermeijer, Martinus F, Andersson, Stefan, de Jong, Frank H, Kayserili, Hülya, de Vroede, Monique A, Otten, Barto J, Rouwé, Catrienus W, Mendonça, Berenice B, Rodrigues, Cidade, Bode, Hans H, de Ruiter, Petra E, Delemarre-van de Waal, Henriette A, Drop, Stenvert L. S

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