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Frontiers in Endocrinology|October 2, 2019
Reversion SAMD9 Mutations Modifying Phenotypic Expression of MIRAGE Syndrome and Allowing Inheritance in a Usually de novo DisorderFlorence Roucher-Boulez, Delphine Mallet, Nicolas Chatron, et al.European Journal of Medical Genetics|November 16, 2019
Mayer-Rokitansky-Künster-Hauser syndrome due to 2q12.1q14.1 deletion: PAX8 the causing gene?Thomas Smol, Wassila Ribero-Karrouz, Patrick Edery, et al.Best Practice & Research. Clinical Endocrinology & Metabolism|June 15, 2010
Surgical options in disorders of sex development (dsd) with ambiguous genitaliaIsabelle Vidal, Daniela Brindusa Gorduza, Elodie Haraux, et al.Bulletin Du Cancer|March 27, 2019
[Atypical genital development and tumor risk]Cécile Faure Conter, Daniela Brindusa Gorduza, Pierre-Yves Mure, et al.Endocrine Connections|January 6, 2023
Changes in the clinical management of 5α-reductase type 2 and 17β-hydroxysteroid dehydrogenase type 3 deficiencies in FranceEstelle Bonnet, Mathias Winter, Delphine Mallet, et al.Journal of Pediatric Urology|May 3, 2016
Surgery in disorders of sex development (DSD) with a gender issue: If (why), when, and how?Pierre D E Mouriquand, Daniela Brindusa Gorduza, Claire-Lise Gay, et al.Pageof 1