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Epigenetics Volume 13, 2018 - Issue 9
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Research Paper

Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders

L. FontanaLaboratory of Molecular Pathology, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milano, ItalyCorrespondence[email protected]
ORCID Iconhttp://orcid.org/0000-0001-9517-6997View further author information
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M. F. BedeschiClinical Genetics Unit, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milano, ItalyView further author information
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S. MaitzClinical Pediatric, Genetics Unit, MBBM Foundation, San Gerardo Monza, Monza, ItalyView further author information
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A. CeredaMedical Genetics Unit, Papa Giovanni XXIII Hospital, Bergamo, ItalyView further author information
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C. FaréDivision of Pathology, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milano, ItalyView further author information
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S. MottaDivision of Pathology, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milano, ItalyView further author information
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A. SeresiniMedical Genetics Laboratory, Fondazione IRCCS Ca’ Granda - Ospedale Maggiore Policlinico, Milano, Italy;Fondazione Grigioni per il Morbo di Parkinson, Milano, ItalyView further author information
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P. D’UrsiDepartment of Biomedical Sciences National Research Council, Institute for Biomedical Technologies, Segrate, ItalyView further author information
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A. OrroDepartment of Biomedical Sciences National Research Council, Institute for Biomedical Technologies, Segrate, ItalyORCID Iconhttp://orcid.org/0000-0002-2581-9579View further author information
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V. PecileMedical Genetics Division, Institute for maternal and child health IRCCS Burlo Garofolo, Trieste, ItalyView further author information
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M. CalvelloDivision of Pathology, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milano, Italy;Division of Cancer Prevention and Genetics, IEO, European Institute of Oncology IRCCS, Milano, ItalyView further author information
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A. SelicorniUOC Pediatria, ASST Lariana, Como, ItalyView further author information
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F. LalattaClinical Genetics Unit, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milano, ItalyView further author information
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D. MilaniPediatric Highly Intensive Care Unit, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milano, ItalyORCID Iconhttp://orcid.org/0000-0002-3087-8514View further author information
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S. M. SirchiaMedical Genetics, Department of Health Sciences, Università degli Studi di Milano, Milano, ItalyORCID Iconhttp://orcid.org/0000-0002-6106-3721View further author information
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M. MiozzoLaboratory of Molecular Pathology, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milano, Italy;Division of Pathology, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milano, ItalyORCID Iconhttp://orcid.org/0000-0002-6523-4575View further author information
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S. TabanoLaboratory of Molecular Pathology, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milano, ItalyORCID Iconhttp://orcid.org/0000-0002-5260-6691View further author information
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Pages 897-909 | Received 26 Apr 2018, Accepted 10 Aug 2018, Published online: 21 Oct 2018

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