Dental agenesis is the most common developmental anomaly in humans and is frequently
associated with several other oral abnormalities. Whereas the incidence of missing teeth …

Dental anomalies are common congenital malformations that can occur either as isolated
findings or as part of a syndrome. This review focuses on genetic causes of abnormal tooth …

In this study, we sought to determine the association between tooth agenesis and DNA
sequence variation in the genes MSX1 and PAX9 in an ethnically diverse human …

The congenital absence of teeth is one of the commonest developmental abnormalities seen
in human populations. Familial hypodontia or oligodontia represents an absence of varying …

Structured Abstract Author–Hitesh Kapadia, Gabriele Mues, Rena D'Souza The
development of dentition is a fascinating process that encompasses a complex series of …

Can kindreds with tooth agenesis caused by MSX1 or PAX9 mutations be distinguished by
their phenotypes? We have identified an MSX1 second bicuspids and mandibular central …

In humans, inherited variation in the number, size, and shape of teeth within the dentitions
are relatively common, while rarer defects of hard tissue formation, including amelogenesis …

Tooth agenesis or hypodontia is one of the most common anomalies of the human dentition,
characterized by the developmental absence of one or more teeth. Many studies have …

Teeth organogenesis develops through a well-ordered series of inductive events involving
genes and BMP, FGF, SHH and WNT represent the main signalling pathways that regulate …

Tooth development is under strict genetic control. Oligodontia is defined as the congenital
absence of 6 or more permanent teeth, excluding the third molar. The occurrence of non …