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Genome-wide paternal uniparental disomy as a cause of Beckwith-Wiedemann syndrome associated with recurrent virilizing adrenocortical tumors.
Bertoin, F; Letouzé, E; Grignani, P; Patey, M; Rossignol, S; Libé, R; Pasqual, C; Lardière-Deguelte, S; Hoeffel-Fornes, C; Gaillard, D; Previderè, C; Delemer, B; Lalli, E.
Afiliación
  • Bertoin F; Department of Endocrinology, CHU Reims, Hôpital Robert Debré, Reims, France.
  • Letouzé E; Programme Cartes d'Identité des Tumeurs, Ligue Nationale contre le Cancer, Paris, France.
  • Grignani P; Department of Public Health, Experimental and Forensic Medicine, University of Pavia, Pavia, Italy.
  • Patey M; Department of Pathology, CHU Reims, Hôpital Robert Debré, Reims, France.
  • Rossignol S; Laboratory of Endocrine Functional Explorations, APHP, Hôpital Armand Trousseau, INSERM UMRS 938 Team 4, Université Pierre et Marie Curie-Paris, Faculté de Médecine, Paris, France.
  • Libé R; Department of Endocrinology-Metabolism-Cancer, APHP, Institut Cochin, Université Paris V-René Descartes, Paris, France.
  • Pasqual C; Service of Diabetology, Hospital of Troyes, Troyes, France.
  • Lardière-Deguelte S; Department of Endocrine Surgery, CHU Reims, Hôpital Robert Debré, Reims, France.
  • Hoeffel-Fornes C; Department of Radiology, CHU Reims, Hôpital Robert Debré, Reims, France.
  • Gaillard D; Department of Genetics, CHU Reims, Hôpital Robert Debré, Reims, France.
  • Previderè C; Department of Public Health, Experimental and Forensic Medicine, University of Pavia, Pavia, Italy.
  • Delemer B; Department of Endocrinology, CHU Reims, Hôpital Robert Debré, Reims, France.
  • Lalli E; Institut de Pharmacologie Moléculaire et Cellulaire, CNRS UMR7275, Sophia Antipolis-Valbonne, France.
Horm Metab Res ; 47(7): 497-503, 2015 Jun.
Article en En | MEDLINE | ID: mdl-25365508
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Virilismo / Síndrome de Beckwith-Wiedemann / Neoplasias de la Corteza Suprarrenal / Disomía Uniparental Tipo de estudio: Risk_factors_studies Límite: Adolescent / Adult / Female / Humans Idioma: En Revista: Horm Metab Res Año: 2015 Tipo del documento: Article País de afiliación: Francia
Texto completo
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PubMed Links
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Virilismo / Síndrome de Beckwith-Wiedemann / Neoplasias de la Corteza Suprarrenal / Disomía Uniparental Tipo de estudio: Risk_factors_studies Límite: Adolescent / Adult / Female / Humans Idioma: En Revista: Horm Metab Res Año: 2015 Tipo del documento: Article País de afiliación: Francia