Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome
O'Sullivan, James ; Bitu, Carolina C. ; Daly, Sarah B. ; Urquhart, Jill E. ; Barron, Martin J. ; Bhaskar, Sanjeev S. ; Martelli-Júnior, Hercilio ; dos Santos Neto, Pedro Eleuterio ; Mansilla, Maria A. ; Murray, Jeffrey C. ; Coletta, Ricardo D. ; Black, Graeme C.M. ; Dixon, Michael J.
American journal of human genetics, 2011-05, Vol.88 (5), p.616-620 [Periódico revisado por pares]Cambridge, MA: Elsevier Inc
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