Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome
- 13 May 2011
- journal article
- research article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 88 (5), 616-620
- https://doi.org/10.1016/j.ajhg.2011.04.005
Abstract
No abstract availableKeywords
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