Functional analysis of Ectodysplasin-A mutations causing selective tooth agenesis

G Mues, A Tardivel, L Willen, H Kapadia… - European Journal of …, 2010 - nature.com
Mutations of the Ectodysplasin-A (EDA) gene are generally associated with the syndrome
hypohidrotic ectodermal dysplasia (MIM 305100), but they can also manifest as selective …

Familial aggregation of maxillary lateral incisor agenesis

T Pinho, P Maciel, C Lemos… - Journal of dental …, 2010 - journals.sagepub.com
In spite of recent developments, data regarding the genes responsible for the less severe
forms of hypodontia are still scarce and controversial. This study addressed the hypothesis …

A novel missense mutation in the ectodysplasinA (EDA) gene underlies Xlinked recessive nonsyndromic hypodontia

M Ayub, F UrRehman, M Yasinzai… - International journal of …, 2010 - Wiley Online Library
Background Nonsyndromic hypodontia or congential absence of one or more permanent
teeth is a common anomaly of dental development in humans. This condition may be …

[PDF][PDF] Missense mutation of the EDA gene in a Jordanian family with X-linked hypohidrotic ectodermal dysplasia: phenotypic appearance and speech problems

OF Khabour, FS Mesmar, F Al-Tamimi… - Genetics and Molecular …, 2010 - Citeseer
Mutations in the EDA gene are responsible for X-linked hypohidrotic ectodermal dysplasia,
the most common form of ectodermal dysplasia. Males show a severe form of this disease …

Familial aggregation of maxillary lateral incisor agenesis

P Maciel, T Pinho, C Lemos, A Sousa - 2010 - repositorium.sdum.uminho.pt
In spite of recent developments, data regarding the genes responsible for the less severe
forms of hypodontia are still scarce and controversial. This study addressed the hypothesis …

[引用][C] 非综合征型先天缺牙的研究进展

施华丽, 刘丽 - 现代口腔医学杂志, 2010