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Rathee Manu
India
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Background: Oligodontia is a genetic disorder which represents the congenital absence of more than six teeth in primary, permanent or both dentitions. It is usually a part of a syndrome and seldom occurs as an isolated entity. Genes responsible for non syndromic oligodontia are found to be MSX1 and PAX9 genes. Methods: Karyotyping was done taking ... Read More»
Rathee Manu, Goel Mahesh, Kumar Arun, Mehta Richa and Kundu Renu
Case Report: J Interdiscipl Med Dent Sci 2014, 2: 117
DOI: 10.4172/2376-032X.1000117
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