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Persistent Müllerian duct syndrome associated with genetic defects in the regulatory subunit of myosin phosphatase.
Picard, Jean-Yves; Morin, Gilles; Devouassoux-Shisheboran, Mojgan; Van der Smagt, Jasper; Klosowski, Serge; Pienkowski, Catherine; Pierre-Renoult, Peggy; Masson, Cécile; Bole, Christine; Josso, Nathalie.
Afiliação
  • Picard JY; Sorbonne Université, INSERM, Centre de Recherches Saint-Antoine, Lipodystrophies, Adaptations Métaboliques et Hormonales et Vieillissement, UMR_S 938, Paris, France.
  • Morin G; Department of Medical Genetics, Centre Hospitalo-Universitaire d'Amiens, Amiens, France.
  • Devouassoux-Shisheboran M; Institut Multisite de Pathologie, Hospices Civils de Lyon, Lyon, France.
  • Van der Smagt J; Division of Clinical Genetics, Medical University of Utrecht, The Netherlands.
  • Klosowski S; Service de Néonatologie, Centre Universitaire de Lens, Lens, France.
  • Pienkowski C; Pathologies Gynécologiques Rares, Hôpital des Enfants, Toulouse Cedex 9, France.
  • Pierre-Renoult P; Unité d'Endocrinologie, CHU Bretonneau, Tours Cedex 9, France.
  • Masson C; Bioinformatics Core Facility, Institut Imagine-Structure Fédérative de Recherche Necker, INSERM U1163 et INSERM US24/CNRS UAR3633, Paris Descartes University, Sorbonne Paris Cite University, Paris, France.
  • Bole C; Genomics Core Facility, Institut Imagine, Structure Fédérative de Recherche Necker, INSERM 1163, INSERM US24/CNRS UAR3633, Paris Descartes University, Sorbonne Paris Cité University, Paris, France.
  • Josso N; Sorbonne Université, INSERM, Centre de Recherches Saint-Antoine, Lipodystrophies, Adaptations Métaboliques et Hormonales et Vieillissement, UMR_S 938, Paris, France.
Hum Reprod ; 37(12): 2952-2959, 2022 11 24.
Article em En | MEDLINE | ID: mdl-36331510
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno 46,XY do Desenvolvimento Sexual Tipo de estudo: Risk_factors_studies Limite: Humans / Male Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno 46,XY do Desenvolvimento Sexual Tipo de estudo: Risk_factors_studies Limite: Humans / Male Idioma: En Ano de publicação: 2022 Tipo de documento: Article