Researchclopedia
Research
Researchers
Institutions
Topics
Submit
About
Search...
⌘
K
Command Palette
Search for a command to run...
Back to research
Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome
2011
161 citations
Journal Article
bronze Open Access
Field-Weighted Citation Impact:
12.68
·
Universidade Estadual de Montes Claros
Pedro Eleuterio dos Santos Neto
·
Universidade Estadual de Montes Claros
M. Adela Mansilla
·
University of Iowa
Jeffrey C. Murray
·
University of Iowa
Ricardo D. Coletta
·
Universidade Estadual de Campinas (UNICAMP)
Graeme C. Black
·
Manchester Academic Health Science Centre
Michael J. Dixon
·
Manchester Academic Health Science Centre
Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome | Researchclopedia