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Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome.
Rooney, Kathleen; Levy, Michael A; Haghshenas, Sadegheh; Kerkhof, Jennifer; Rogaia, Daniela; Tedesco, Maria Giovanna; Imperatore, Valentina; Mencarelli, Amedea; Squeo, Gabriella Maria; Di Venere, Eleonora; Di Cara, Giuseppe; Verrotti, Alberto; Merla, Giuseppe; Tedder, Matthew L; DuPont, Barbara R; Sadikovic, Bekim; Prontera, Paolo.
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  • Rooney K; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A 3K7, Canada.
  • Levy MA; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON N6A 5W9, Canada.
  • Haghshenas S; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON N6A 5W9, Canada.
  • Kerkhof J; Department of Pathology and Laboratory Medicine, Western University, London, ON N6A 3K7, Canada.
  • Rogaia D; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON N6A 5W9, Canada.
  • Tedesco MG; Medical Genetics Unit, Maternal-Infantile Department, University and Hospital of Perugia, 06129 Perugia, Italy.
  • Imperatore V; Pediatric Clinic, Department of Medicine, University of Perugia, 06129 Perugia, Italy.
  • Mencarelli A; Medical Genetics Unit, Maternal-Infantile Department, University and Hospital of Perugia, 06129 Perugia, Italy.
  • Squeo GM; Medical Genetics Unit, Maternal-Infantile Department, University and Hospital of Perugia, 06129 Perugia, Italy.
  • Di Venere E; Medical Genetics Unit, Maternal-Infantile Department, University and Hospital of Perugia, 06129 Perugia, Italy.
  • Di Cara G; Pediatric Clinic, Department of Medicine, University of Perugia, 06129 Perugia, Italy.
  • Verrotti A; Laboratory of Regulatory and Functional Genomics, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, Italy.
  • Merla G; Laboratory of Regulatory and Functional Genomics, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, Italy.
  • Tedder ML; Pediatric Clinic, Department of Medicine, University of Perugia, 06129 Perugia, Italy.
  • DuPont BR; Pediatric Clinic, Department of Medicine, University of Perugia, 06129 Perugia, Italy.
  • Sadikovic B; Laboratory of Regulatory and Functional Genomics, Fondazione IRCCS Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo, Italy.
  • Prontera P; Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, 80100 Naples, Italy.
Int J Mol Sci ; 22(16)2021 Aug 10.
Article en En | MEDLINE | ID: mdl-34445317
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Metilación de ADN / Síndrome de DiGeorge / Epigenoma Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Infant / Male Idioma: En Revista: Int J Mol Sci Año: 2021 Tipo del documento: Article País de afiliación: Canadá
Texto completo
Añadir a Mi BVS
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Metilación de ADN / Síndrome de DiGeorge / Epigenoma Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Infant / Male Idioma: En Revista: Int J Mol Sci Año: 2021 Tipo del documento: Article País de afiliación: Canadá