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The Application of Clinical Genetics Volume 7, 2014 - Issue

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Beckwith–Wiedemann and IMAGe syndromes: two very different diseases caused by mutations on the same gene

Donatella Milani1 Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Italy

Lidia Pezzani1 Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Italy

Silvia Tabano2 Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Italy

Monica Miozzo2 Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Italy;3 Division of Pathology, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milan, ItalyCorrespondence[email protected]

Pages 169-175 | Published online: 16 Sep 2014

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Susanna Esposito, Marta Cerutti, Donatella Milani, Francesca Menni & Nicola Principi. (2016) Vaccination coverage of children with rare genetic diseases and attitudes of their parents toward vaccines. Human Vaccines & Immunotherapeutics 12:3, pages 801-805.
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Leda Paganini, Nicole Carlessi, Laura Fontana, Rosamaria Silipigni, Silvia Motta, Stefano Fiori, Silvana Guerneri, Faustina Lalatta, Anna Cereda, Silvia Sirchia, Monica Miozzo & Silvia Tabano. (2015) Beckwith–Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi. Epigenetics 10:7, pages 643-649.
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