Publication
Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome
Anneke Kievit, Federico Tessadori, Hannie Douben, Ingrid Jordens, Madelon Maurice, Jeannette Hoogeboom, Raoul Hennekam, Sheela Nampoothiri, Hülya Kayserili, Marco Castori, Margo Whiteford, Connie Motter, Catherine Melver, Michael Cunningham, Anne Hing, Nancy M. Kokitsu-Nakata, Siulan Vendramini-Pittoli, Antonio Richieri-Costa, Annette F. Baas, Corstiaan C. Breugem, Karen Duran, Maarten Massink, Patrick W. B. Derksen, Wilfred F. J. van IJcken, Leontine van Unen, Fernando Santos-Simarro, Pablo Lapunzina, Vera L. Gil-da Silva Lopes, Elaine Lustosa-Mendes, Max Krall, Anne Slavotinek, Victor Martinez-Glez, Jeroen Bakkers, Koen L. I. van Gassen, Annelies de Klein, Marie-José H. van den Boogaard, Gijs van Haaften
European Journal of Human Genetics, January 2018, Springer Science + Business Media
DOI: 10.1038/s41431-017-0010-5