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Showing 1 - 13 of 18

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  • New NR5A1 mutations and phenotypic variations of gonadal dysgenesis

    Ralf Werner, Isabel Mönig, Ralf Lünstedt, Lutz Wünsch, Christoph Thorns, Benedikt Reiz, Alexandra Krause, Karl Otfried Schwab, Gerhard Binder, Paul-Martin Holterhus, Olaf Hiort

    published 01 May 2017

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  • Human MAMLD1 Gene Variations Seem Not Sufficient to Explain a 46,XY DSD Phenotype

    Núria Camats, Mónica Fernández-Cancio, Laura Audí, Primus E. Mullis, Francisca Moreno, Isabel González Casado, Juan Pedro López-Siguero, Raquel Corripio, José Antonio Bermúdez de la Vega, José Antonio Blanco, Christa E. Flück

    published 16 Nov 2015

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