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Plos One|December 20, 2012
Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6Jan C-C Hu, Hui-Chen Chan, Stephen G Simmer, et al.Journal of Radiological Protection : Official Journal of the Society for Radiological Protection|April 15, 2014
Mitigating the risk of radiation-induced cancers: limitations and paradigms in drug developmentStephen S Yoo, Timothy J Jorgensen, Ann R Kennedy, et al.Journal of Dental Research|March 20, 2018
Hypoplastic AI with Highly Variable Expressivity Caused by ENAM MutationsM Koruyucu, J Kang, Y J Kim, et al.Molecular Genetics & Genomic Medicine|January 29, 2015
Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindredsJie Yang, Shih-Kai Wang, Murim Choi, et al.International Journal of Oral Science|October 1, 2021
Analyses of oligodontia phenotypes and genetic etiologiesMengqi Zhou, Hong Zhang, Heather Camhi, et al.Molecular Genetics & Genomic Medicine|January 21, 2016
Fam83h null mice support a neomorphic mechanism for human ADHCAIShih-Kai Wang, Yuanyuan Hu, Jie Yang, et al.Clinical Genetics|December 4, 2018
Mutations in RELT cause autosomal recessive amelogenesis imperfectaJung-Wook Kim, Hong Zhang, Figen Seymen, et al.Journal of Dental Research|October 13, 2010
Novel WDR72 mutation and cytoplasmic localizationS-K Lee, F Seymen, K-E Lee, et al.Molecular Genetics & Genomic Medicine|June 5, 2020
Dental malformations associated with biallelic MMP20 mutationsShih-Kai Wang, Hong Zhang, Michael B Chavez, et al.Genes|May 28, 2022
The Modified Shields Classification and 12 Families with Defined DSPP MutationsJames P Simmer, Hong Zhang, Sophie J H Moon, et al.Pageof 24