Browsing by Author Urquhart, JE
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Preview | Issue Date | Title | Author(s) | Advisor | Type |
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2011 | Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome | O'Sullivan, J; Bitu, CC; Daly, SB; Urquhart, JE; Barron, MJ; Bhaskar, SS; Martelli, H; Neto, PED; Mansilla, MA; Murray, JC; Coletta, RD; Black, GCM; Dixon, MJ | - | Artigo de periódico |