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Erratum to: A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.
Russo, Silvia; Calzari, Luciano; Mussa, Alessandro; Mainini, Ester; Cassina, Matteo; Di Candia, Stefania; Clementi, Maurizio; Guzzetti, Sara; Tabano, Silvia; Miozzo, Monica; Sirchia, Silvia; Finelli, Palma; Prontera, Paolo; Maitz, Silvia; Sorge, Giovanni; Calcagno, Annalisa; Maghnie, Mohamad; Divizia, Maria Teresa; Melis, Daniela; Manfredini, Emanuela; Ferrero, Giovanni Battista; Pecile, Vanna; Larizza, Lidia.
Afiliación
  • Russo S; Human Molecular Genetics Laboratory, IRCCS Istituto Auxologico Italiano, Milano, Italy.
  • Calzari L; Human Molecular Genetics Laboratory, IRCCS Istituto Auxologico Italiano, Milano, Italy.
  • Mussa A; Department of Pediatric and Public Health Sciences, University of Turin, Torino, Italy.
  • Mainini E; Human Molecular Genetics Laboratory, IRCCS Istituto Auxologico Italiano, Milano, Italy.
  • Cassina M; Clinical Genetics Unit, Department of Women's and Children's Health, University of Padua, Padova, Italy.
  • Di Candia S; Department of Pediatrics, San Raffaele Scientific Institute, Milano, Italy.
  • Clementi M; Clinical Genetics Unit, Department of Women's and Children's Health, University of Padua, Padova, Italy.
  • Guzzetti S; Human Molecular Genetics Laboratory, IRCCS Istituto Auxologico Italiano, Milano, Italy.
  • Tabano S; Division of Pathology - Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Department of Pathophysiology and Transplantation, University of Milan, Milano, Italy.
  • Miozzo M; Division of Pathology - Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Department of Pathophysiology and Transplantation, University of Milan, Milano, Italy.
  • Sirchia S; Department of Health Sciences, University of Milan, Milano, Italy.
  • Finelli P; Human Molecular Genetics Laboratory, IRCCS Istituto Auxologico Italiano, Milano, Italy.
  • Prontera P; Medical Genetics Unit, Department of Surgical and Biomedical Sciences, University of Perugia, Hospital "S. M. della Misericordia", Perugia, Italy.
  • Maitz S; Clinical Pediatric Genetics Unit, Pediatrics Clinics, MBBM Foundation, S. Gerardo Hospital, Monza, Italy.
  • Sorge G; Department of Pediatrics and Medical Sciences, AO "Policlinico Vittorio Emanuele", Catania, Italy.
  • Calcagno A; Pediatric Endocrine Unit, Department of Pediatrics, IRCCS, Children's Hospital Giannina Gaslini, Genova, Italy.
  • Maghnie M; Pediatric Endocrine Unit, Department of Pediatrics, IRCCS, Children's Hospital Giannina Gaslini, Genova, Italy.
  • Divizia MT; Department of Neuroscience, Rehabilitation, Ophtalmology, Genetics, Maternal and Child Health, University of Genova, Genova, Italy.
  • Melis D; Department of Medical Genetics, IRCCS, Children's Hospital Giannina Gaslini, Genova, Italy.
  • Manfredini E; Clinical Pediatric Genetics, Department of Pediatrics, University "Federico II", Napoli, Italy.
  • Ferrero GB; Medical Genetics Unit, Department of Laboratory Medicine, Niguarda Ca' Granda Hospital, Milano, Italy.
  • Pecile V; Department of Pediatric and Public Health Sciences, University of Turin, Torino, Italy.
  • Larizza L; Institute for Maternal and Child Health, Foundation IRCCS Burlo Garofolo Institute, Trieste, Italy.
Clin Epigenetics ; 8: 40, 2016.
Article en En | MEDLINE | ID: mdl-27110297
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Clin Epigenetics Año: 2016 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Alemania
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Clin Epigenetics Año: 2016 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Alemania