MSX 1 gene variant and non-syndromic clefting: Association or rejection?

Conclusions: From a genetically diverse etiology MSX 1 799 G >T gene variant may be a good screening marker for NSCL/P in Raichur patients.
Source: Table of Contents : Indian Journal of Dental Research : 2006 - 17(3) - Category: Dentistry Authors: Source Type: research