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Fetal growth patterns in Beckwith-Wiedemann syndrome.
Mussa, A; Russo, S; de Crescenzo, A; Freschi, A; Calzari, L; Maitz, S; Macchiaiolo, M; Molinatto, C; Baldassarre, G; Mariani, M; Tarani, L; Bedeschi, M F; Milani, D; Melis, D; Bartuli, A; Cubellis, M V; Selicorni, A; Silengo, M C; Larizza, L; Riccio, A; Ferrero, G B.
Afiliação
  • Mussa A; Department of Pediatric and Public Health Sciences, University of Turin, Turin, Italy.
  • Russo S; Laboratory of Cytogenetics and Molecular Genetics, Istituto Auxologico Italiano, Milan, Italy.
  • de Crescenzo A; DiSTABiF, Second University of Naples, Naples, Italy.
  • Freschi A; DiSTABiF, Second University of Naples, Naples, Italy.
  • Calzari L; Laboratory of Cytogenetics and Molecular Genetics, Istituto Auxologico Italiano, Milan, Italy.
  • Maitz S; Clinical Pediatric Genetics Unit, Pediatrics Clinics, MBBM Foundation, S. Gerardo Hospital, Monza, Italia.
  • Macchiaiolo M; Rare Disease and Medical Genetics Unit, Bambino Gesù Children Hospital, Rome, Italy.
  • Molinatto C; Department of Pediatric and Public Health Sciences, University of Turin, Turin, Italy.
  • Baldassarre G; Department of Pediatric and Public Health Sciences, University of Turin, Turin, Italy.
  • Mariani M; Clinical Pediatric Genetics Unit, Pediatrics Clinics, MBBM Foundation, S. Gerardo Hospital, Monza, Italia.
  • Tarani L; Department of Pediatric and Pediatric Neuropsychiatry, Sapienza University, Rome, Italy.
  • Bedeschi MF; Medical Genetics Unit, IRCCS Ca' Granda Foundation, Ospedale Maggiore Policlinico, Milan, Italy.
  • Milani D; Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, Università degli Studi di Milano Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
  • Melis D; Clinical Pediatric Genetics, Department of Pediatrics, University "Federico II", Naples, Italy.
  • Bartuli A; Rare Disease and Medical Genetics Unit, Bambino Gesù Children Hospital, Rome, Italy.
  • Cubellis MV; Department of Biology, University of Naples Federico II, Naples, Italy.
  • Selicorni A; Clinical Pediatric Genetics Unit, Pediatrics Clinics, MBBM Foundation, S. Gerardo Hospital, Monza, Italia.
  • Silengo MC; Department of Pediatric and Public Health Sciences, University of Turin, Turin, Italy.
  • Larizza L; Laboratory of Cytogenetics and Molecular Genetics, Istituto Auxologico Italiano, Milan, Italy.
  • Riccio A; DiSTABiF, Second University of Naples, Naples, Italy.
  • Ferrero GB; Institute of Genetics and Biophysics "A. Buzzati-Traverso" - CNR, Naples, Italy.
Clin Genet ; 90(1): 21-7, 2016 Jul.
Article em En | MEDLINE | ID: mdl-26857110
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Beckwith-Wiedemann / Impressão Genômica / Metilação de DNA / Dissomia Uniparental / Desenvolvimento Fetal / Inibidor de Quinase Dependente de Ciclina p57 Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Beckwith-Wiedemann / Impressão Genômica / Metilação de DNA / Dissomia Uniparental / Desenvolvimento Fetal / Inibidor de Quinase Dependente de Ciclina p57 Idioma: En Ano de publicação: 2016 Tipo de documento: Article