Tooth agenesis is one of the most prevalent craniofacial congenital anomalies found in
some people. Some genes, such as homeobox gene (MSX1), paired domain transcription …

Tooth agenesis is the most prevalent craniofacial congenital anomaly in humans. The term
refers to an isolated disorder in the absence of non-dental phenotypes but is also used to …

Objectives: The main focus of this review article was to collate up to date knowledge with
regard to significance of single nucleotide polymorphisms (SNPs) in various genes …

Tooth agenesis is one of the most common congenital malformations in humans.
Hypodontia can either occur as an isolated condition (non-syndromic hypodontia) or can be …

Background: Tooth agenesis is one of the most common developmental anomalies in
human, which one or a few teeth are absent because they have never formed, may cause …

Tooth agenesis denotes a condition where teeth are missing due to a developmental failure.
According to severity, this malformation can be subdivided into hypodontia, oligodontia and …

Tooth agenesis in human being is the most common congenital anomaly associated with
dental development. Mutations in many genes such as MSH homeobox 1 (MSX1), paired …

Background Dental agenesis is the most common developmental anomaly in man and may
present either as an isolated trait or as part of a syndrome, such as ectodermal dysplasia …

Tooth agenesis is one of the most common developmental disorders in humans. Previous
studies have attributed non‐syndromic tooth agenesis to mutations in several genes …

Tooth agenesis constitutes the most common anomalies of dental development in man.
Despite this, little is known about the genetic defects responsible for this complex condition …