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Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders.
Fontana, L; Bedeschi, M F; Maitz, S; Cereda, A; Faré, C; Motta, S; Seresini, A; D'Ursi, P; Orro, A; Pecile, V; Calvello, M; Selicorni, A; Lalatta, F; Milani, D; Sirchia, S M; Miozzo, M; Tabano, S.
Afiliação
  • Fontana L; a Laboratory of Molecular Pathology, Department of Pathophysiology and Transplantation , Università degli Studi di Milano , Milano , Italy.
  • Bedeschi MF; b Clinical Genetics Unit , Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico , Milano , Italy.
  • Maitz S; c Clinical Pediatric, Genetics Unit , MBBM Foundation, San Gerardo Monza , Monza , Italy.
  • Cereda A; d Medical Genetics Unit , Papa Giovanni XXIII Hospital , Bergamo , Italy.
  • Faré C; e Division of Pathology , Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico , Milano , Italy.
  • Motta S; e Division of Pathology , Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico , Milano , Italy.
  • Seresini A; f Medical Genetics Laboratory , Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico , Milano , Italy.
  • D'Ursi P; g Fondazione Grigioni per il Morbo di Parkinson , Milano , Italy.
  • Orro A; h Department of Biomedical Sciences National Research Council , Institute for Biomedical Technologies , Segrate , Italy.
  • Pecile V; h Department of Biomedical Sciences National Research Council , Institute for Biomedical Technologies , Segrate , Italy.
  • Calvello M; i Medical Genetics Division , Institute for maternal and child health IRCCS Burlo Garofolo , Trieste , Italy.
  • Selicorni A; e Division of Pathology , Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico , Milano , Italy.
  • Lalatta F; j Division of Cancer Prevention and Genetics, IEO , European Institute of Oncology IRCCS , Milano , Italy.
  • Milani D; k UOC Pediatria , ASST Lariana , Como , Italy.
  • Sirchia SM; b Clinical Genetics Unit , Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico , Milano , Italy.
  • Miozzo M; l Pediatric Highly Intensive Care Unit , Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico , Milano , Italy.
  • Tabano S; m Medical Genetics, Department of Health Sciences , Università degli Studi di Milano , Milano , Italy.
Epigenetics ; 13(9): 897-909, 2018.
Article em En | MEDLINE | ID: mdl-30221575
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Beckwith-Wiedemann / Cromossomos Humanos Par 15 / Impressão Genômica / Metilação de DNA / Síndrome de Silver-Russell Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Epigenetics Assunto da revista: GENETICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Itália
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Beckwith-Wiedemann / Cromossomos Humanos Par 15 / Impressão Genômica / Metilação de DNA / Síndrome de Silver-Russell Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Epigenetics Assunto da revista: GENETICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Itália