Paired box 9 (PAX9) is one of the best‐known transcription factors involved in the
development of human dentition. Mutations in PAX9 gene could, therefore, seriously …

Abstract Paired box 9 (PAX9) gene belongs to the PAX family, which encodes a family of
metazoan transcription factors documented by a conserved DNA binding paired domain 128 …

Background: Non-syndromic oligodontia is characterized by the absence of six or more
permanent teeth, excluding third molars, and can have aesthetic, masticatory, and …

Tooth agenesis is one of the most common craniofacial disorders in humans. More than 350
genes have been associated with teeth development. In this study, we enrolled 60 child …

Abstract Studies have reported that> 91.9% of non-syndromic tooth agenesis cases are
caused by seven pathogenic genes. Objective To report novel heterozygous PAX9 variants …

Objective The aim of this study was to investigate the epidemiology of delayed tooth
development (DTD) and the link between DTD and tooth agenesis (TA). Design The dental …

Objective To investigate a novel gene mutation in a Chinese patient with non‐syndromic
hypodontia. Subjects and Methods Mutation analysis was carried out by whole exome …

Objective: To identify the dental anomalies that can modify the occlusal characteristics and
their distribution in these occlusal alterations in the skeletal patterns of children. Material and …

Background The congenital absence of one or few teeth, hypodontia, is considered one of
the utmost dental ageneses in human beings. Several genes have been shown to be …

The present study aimed to determine the genetic variants of PAX9, MSX1, and AXIN2 in
Mayan probands with non-syndromic dental agenesis (NSDA) from Yucatan, Mexico. We …