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2q37 Deletions in Patients With an Albright Hereditary Osteodystrophy Phenotype and PTH Resistance.
Elli, Francesca Marta; de Sanctis, Luisa; Madeo, Bruno; Maffini, Maria A; Bordogna, Paolo; Pirelli, Arianna; Arosio, Maura; Mantovani, Giovanna.
Afiliação
  • Elli FM; Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy.
  • de Sanctis L; Department of Public Health and Pediatric Sciences, Regina Margherita Children's Hospital-AOU Città della Salute e della Scienza, University of Torino, Turin, Italy.
  • Madeo B; Unit of Endocrinology, Department of Medical Specialties, Ospedale Civile di Baggiovara, Azienda Ospedaliero-Universitaria di Modena, Modena, Italy.
  • Maffini MA; Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy.
  • Bordogna P; Endocrinology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
  • Pirelli A; Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy.
  • Arosio M; Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy.
  • Mantovani G; Endocrinology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Front Endocrinol (Lausanne) ; 10: 604, 2019.
Article em En | MEDLINE | ID: mdl-31555217
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2019 Tipo de documento: Article