Now showing items 1-2 of 2
The evolution of the nosology of osteogenesis imperfecta
(Wiley-Blackwell, 2021)
Osteogenesis imperfecta (OI) is a relatively common genetic skeletal disorder with an estimated frequency of 1 in 20 000 worldwide. The manifestations are diverse and although individually rare, the several different forms ...
Taurodontism in dental genetics
(Springer Nature, 2021)
Taurodontism is a dental anomaly defined by enlargement of the pulp chamber of multirooted teeth with apical displacement of
the pulp floor and bifurcation of the roots. Taurodontism can be an isolated trait or part of a ...