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Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum.
Passaretti, Francesco; Pignata, Laura; Vitiello, Giuseppina; Alesi, Viola; D'Elia, Gemma; Cecere, Francesco; Acquaviva, Fabio; De Brasi, Daniele; Novelli, Antonio; Riccio, Andrea; Iolascon, Achille; Cerrato, Flavia.
Afiliação
  • Passaretti F; Department of Molecular Medicine and Medical Biotechnology, Università degli Studi di Napoli Federico II, 80131 Naples, Italy.
  • Pignata L; U.O.C. Medical Genetics, Department of Translational Medical Sciences, A.O.U. Federico II, 80131 Naples, Italy.
  • Vitiello G; Department of Environmental Biological and Pharmaceutical Sciences and Technologies (DiSTABiF), Università degli Studi della Campania "Luigi Vanvitelli", 81100 Caserta, Italy.
  • Alesi V; U.O.C. Medical Genetics, Department of Translational Medical Sciences, A.O.U. Federico II, 80131 Naples, Italy.
  • D'Elia G; Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children Hospital, IRCCS, 00165 Rome, Italy.
  • Cecere F; Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children Hospital, IRCCS, 00165 Rome, Italy.
  • Acquaviva F; Department of Environmental Biological and Pharmaceutical Sciences and Technologies (DiSTABiF), Università degli Studi della Campania "Luigi Vanvitelli", 81100 Caserta, Italy.
  • De Brasi D; Institute of Genetics and Biophysics (IGB) "Adriano Buzzati-Traverso", Consiglio Nazionale delle Ricerche (CNR), 80131 Naples, Italy.
  • Novelli A; U.O.S. Medical Genetics, Pediatrics of Chronic and Multifactorial Diseases, A.O.R.N. Santobono-Pausilipon, 80129 Naples, Italy.
  • Riccio A; U.O.S. Medical Genetics, Pediatrics of Chronic and Multifactorial Diseases, A.O.R.N. Santobono-Pausilipon, 80129 Naples, Italy.
  • Iolascon A; Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children Hospital, IRCCS, 00165 Rome, Italy.
  • Cerrato F; Department of Environmental Biological and Pharmaceutical Sciences and Technologies (DiSTABiF), Università degli Studi della Campania "Luigi Vanvitelli", 81100 Caserta, Italy.
Genes (Basel) ; 13(10)2022 10 16.
Article em En | MEDLINE | ID: mdl-36292759
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Silver-Russell Limite: Humans Idioma: En Revista: Genes (Basel) Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Silver-Russell Limite: Humans Idioma: En Revista: Genes (Basel) Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Itália