These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
145 related articles for article (PubMed ID: 28473773)
1. Analyses of Kim YJ; Kang J; Seymen F; Koruyucu M; Gencay K; Shin TJ; Hyun HK; Lee ZH; Hu JC; Simmer JP; Kim JW Front Physiol; 2017; 8():229. PubMed ID: 28473773 [TBL] [Abstract][Full Text] [Related]
2. Alteration of Exon Definition Causes Amelogenesis Imperfecta. Kim YJ; Kang J; Seymen F; Koruyucu M; Zhang H; Kasimoglu Y; Bayram M; Tuna-Ince EB; Bayrak S; Tuloglu N; Hu JC; Simmer JP; Kim JW J Dent Res; 2020 Apr; 99(4):410-418. PubMed ID: 31999931 [TBL] [Abstract][Full Text] [Related]
3. Novel MMP20 and KLK4 Mutations in Amelogenesis Imperfecta. Seymen F; Park JC; Lee KE; Lee HK; Lee DS; Koruyucu M; Gencay K; Bayram M; Tuna EB; Lee ZH; Kim YJ; Kim JW J Dent Res; 2015 Aug; 94(8):1063-9. PubMed ID: 26124219 [TBL] [Abstract][Full Text] [Related]
4. Spectrum of pathogenic variants and founder effects in amelogenesis imperfecta associated with MMP20. Nikolopoulos G; Smith CEL; Poulter JA; Murillo G; Silva S; Lamb T; Berry IR; Brown CJ; Day PF; Soldani F; Al-Bahlani S; Harris SA; O'Connell MJ; Inglehearn CF; Mighell AJ Hum Mutat; 2021 May; 42(5):567-576. PubMed ID: 33600052 [TBL] [Abstract][Full Text] [Related]
5. Novel Lee Y; Zhang H; Seymen F; Kim YJ; Kasimoglu Y; Koruyucu M; Simmer JP; Hu JC; Kim JW J Pers Med; 2022 Jan; 12(2):. PubMed ID: 35207639 [TBL] [Abstract][Full Text] [Related]
14. Missense Mutation in Fam83H Gene in Iranian Patients with Amelogenesis Imperfecta. Pourhashemi SJ; Ghandehari Motlagh M; Meighani G; Ebrahimi Takaloo A; Mansouri M; Mohandes F; Mirzaii M; Khoshzaban A; Moshtaghi F; Abedkhojasteh H; Heidari M Iran J Public Health; 2014 Dec; 43(12):1680-7. PubMed ID: 26171361 [TBL] [Abstract][Full Text] [Related]
15. A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family. Khan SA; Khan MA; Muhammad N; Bashir H; Khan N; Muhammad N; Yilmaz R; Khan S; Wasif N BMC Med Genet; 2020 May; 21(1):97. PubMed ID: 32380970 [TBL] [Abstract][Full Text] [Related]
16. Novel KLK4 and MMP20 mutations discovered by whole-exome sequencing. Wang SK; Hu Y; Simmer JP; Seymen F; Estrella NM; Pal S; Reid BM; Yildirim M; Bayram M; Bartlett JD; Hu JC J Dent Res; 2013 Mar; 92(3):266-71. PubMed ID: 23355523 [TBL] [Abstract][Full Text] [Related]