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Korff, Simona; Mostaguir, Khaled; Beghetti, Maurice; D'Antiga, Lorenzo; Debray, Dominique; Franchi-Abella, Stéphanie; Gonzales, Emmanuel; Guerin, Florent; Hachulla, Anne-Lise; Lambert, Virginie; Makrythanasis, Periklis; Roduit, Nicolas; Savale, Laurent; Senat, Marie-Victoire; Spaltenstein, Joël; van Steenbeek, Frank; Wildhaber, Barbara E; Zwahlen, Marcel; McLin, Valérie A (2022). International registry of congenital porto-systemic shunts: a multi-centre, retrospective and prospective registry of neonates, children and adults with congenital porto-systemic shunts. Orphanet journal of rare diseases, 17(1), p. 284. BioMed Central 10.1186/s13023-022-02412-8
Makrythanasis, Periklis; Kapranov, Philipp; Bartoloni, Lucia; Reymond, Alexandre; Deutsch, Samuel; Guigo, Roderic; Denoeud, France; Drenkow, Jorg; Rossier, Colette; Ariani, Francesca; Capra, Valeria; Excoffier, Laurent; Renieri, Alessandra; Gingeras, Thomas R.; Antonarakis, Stylianos E. (2009). Variation in Novel Exons (RACEfrags) of the MECP2 Gene in Rett Syndrome Patients and Controls. Human mutation, 30(9), E866 - E879. Hoboken, N.J.: Wiley-Blackwell 10.1002/humu.21073
