Results 181 to 190 of about 12,486 (245)

A novel missense mutation of the EDA gene in a Mongolian family with congenital hypodontia [PDF]

, 2006
Ran Tao, Buhe Jin, Shen Zheng Guo, Qing Wei, Guo Feng, David G. Brooks, Lijun Liu, Junfu Xu, Tai-Wei Li, Yujuan Yan, Lin He   +10 more
openalex   +1 more source

Heterogeneity of Orodental Features in a Family with Noonan Syndrome. [PDF]

Int J Mol Sci
Antal G, Csabai L, Zsigmond A, Szanto I, Hadzsiev K, Bene J.   +5 more
europepmc   +1 more source

Bilateral and Unilateral Fused Primary Teeth With Hypodontia in Permanent Dentition: A Case Series. [PDF]

Cureus
Budayri RW, Morad M, Alhazmy R, Aljohani AS.   +3 more
europepmc   +1 more source

Taurodontism and related dental anomalies: influence of maternal, prenatal, and postnatal factors in pediatric patients. [PDF]

BMC Oral Health
Ozgur OM, Seyma M, Aynur K, Nazan KT.
europepmc   +1 more source

Case of a Male Patient With Focal Dermal Hypoplasia (Goltz Syndrome), Esophageal Polyps, Scoliosis, and Bicuspid Aortic Valve. [PDF]

Cureus
Stoimenov B, Pancheva R, Pencheva V, Kolev V, Karakasheva R, Stoyanov D, Stancheva M, Tsrancheva R, Donev S, Petrova D, Yordanov V, Vasileva A, Ovnarski G, Genov D.   +13 more
europepmc   +1 more source

Understanding the implications of the PAX9 Gene in tooth development [PDF]

, 2011
Arcuri, C, Muzzi, F, Panetta, V, Santini, F, Squitti, R, Zito, I   +5 more
core   +1 more source

Concomitant hypodontia and hyperodontia—An analysis of nine patients

, 2011
Małgorzata Zadurska, B. Sieminska-Piekarczyk, Dorota Maciejak, Barbera Wyszomirska-Zdybel, Jüri Kurol   +4 more
openalex   +1 more source

Implant treatment modalities of non-syndromic congenitally missing premolars: a retrospective case series of 74 specialist care patients over an 11-year-cohort. [PDF]

Acta Odontol Scand
Hassan SJ, Lappalainen OP, Marleena OA, Harila V, Näpänkangas R.   +4 more
europepmc   +1 more source

Oligodontia Management in a Resource-Limited Setting: Two Case Reports and Review of Literature. [PDF]

Case Rep Dent
Malami AB, Ogbozor BE, Okolo CC, Aborisade AO, Mahmud UB, Abulfathi AA, Adeyemo YI.   +6 more
europepmc   +1 more source

A MISSENSE MUTATION OF MSX1 GENE IN PAKISTANI FAMILIES WITH HYPODONTIA

, 2019
Muhammad Nawaz, Nasrullah Mengal, Shai Mureed, Agha Muhammad Raza, Muhammad Saeed, Jamil Ahmed   +5 more
openalex   +1 more source