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 TitleAuthors / EditorsDate
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Pränatale und genetische Aspekte angeborener Herzerkrankungen Fasnacht, M; Jaeggi, Edgard 2001
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Association of the connexin36 gene with juvenile myoclonic epilepsy Mas, Christophe; Taske, N.; Deutsch, Samuel; Guipponi, Michel; ... Meda, Paolo 2004
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Preimplantation genetic diagnosis and epigenetics?- continued surveillance Giacobino, Ariane 2006
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One-year evaluation of a neonatal screening program for cystic fibrosis in Switzerland Rueegg, Corina S; Kuehni, Claudia E; Gallati, Sabina; Baumgartner, Matthias; ... Barben, Juerg 2013
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Precision medicine for monogenic diabetes: from a survey to the development of a next-generation diagnostic panel Kherra, Sakina; Blouin, Jean-Louis; Santoni, Federico; Schwitzgebel Luscher, Valérie 2017
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Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology Ripperger, Tim; Von Bueren, André 2017
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Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits Evangelou, Evangelos; Warren, Helen R; Mosen-Ansorena, David; Mifsud, Borbala; ... Caulfield, Mark J 2018
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De novo variants in neurodevelopmental disorders with epilepsy Heyne, Henrike O; Singh, Tarjinder; Stamberger, Hannah; Abou Jamra, Rami; ... Lemke, Johannes R 2018
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Parcours diagnostique des patients atteints de maladie de Gaucher de type 1 : enquête auprès de médecins internistes et hématologues Deriaz, S; De Roux Serratrice, Christine; Lidove, O; Noël, E; ... Maillot, F 2019