Tooth agenesis and non-syndromic cleft lip/palate with or without tooth agenesis is often
encountered in clinical practice. Several studies have been done to determine the cause of …

MSX1 has been considered a strong candidate for orofacial clefting, based on mouse
expression studies and knockout models, as well as association and linkage studies in …

Background MSX1 sequence variants have been known to cause human tooth agenesis
(TA) with or without orofacial clefts. However, their roles during the whole processes of tooth …

Introduction. MSX1 gene has a critical role in craniofacial development, the aim of this case–
control study is to test the hypothesis that MSX1 mutation contributes to congenital tooth …

MSX1 gene is among the Homeo box genes. The Master genes that control the downstream
genes and are involved in the patterning of the face. MSX 1 deficient mice have shown to …

Objective: To understand the role of MSX1 gene in Indian nonsyndromic cleft palate
patients. Materials and methods: A cross-sectional study was devised consisting of …

Objective Muscle segment homeobox gene 1 (MSX1) is widely expressed in craniofacial
development and tooth formation. The aim of this study was to report a novel MSX1 mutation …

Aims: The aim of this study is to amplify the chosen region (799 G> T) of MSX 1 gene,
investigate the degree of association and perform a mutation research from Raichur cleft lip …

Objective The aim of this study was to investigate the contribution of 6 polymorphic variants
of the MSX 1 gene in non‐syndromic cleft lip and/or palate (NSCL/P). Methods Three …

Objectives This study investigated the association of MSX1 gene variants rs3821949 and
rs12532 with nonsyndromic cleft lip and/or palate (NSCL/P) in the Pakistani population …