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.
42. A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q24.3. Mendoza G; Pemberton TJ; Lee K; Scarel-Caminaga R; Mehrian-Shai R; Gonzalez-Quevedo C; Ninis V; Hartiala J; Allayee H; Snead ML; Leal SM; Line SR; Patel PI Hum Genet; 2007 Jan; 120(5):653-62. PubMed ID: 17024372 [TBL] [Abstract][Full Text] [Related]
43. The mineral and protein content of enamel in amelogenesis imperfecta. Wright JT; Deaton TG; Hall KI; Yamauchi M Connect Tissue Res; 1995; 32(1-4):247-52. PubMed ID: 7554923 [TBL] [Abstract][Full Text] [Related]
44. Wang YL; Lin HC; Liang T; Lin JC; Simmer JP; Hu JC; Wang SK J Dent Res; 2024 Jun; 103(6):662-671. PubMed ID: 38716742 [TBL] [Abstract][Full Text] [Related]
45. Premature stop codon in MMP20 causing amelogenesis imperfecta. Papagerakis P; Lin HK; Lee KY; Hu Y; Simmer JP; Bartlett JD; Hu JC J Dent Res; 2008 Jan; 87(1):56-9. PubMed ID: 18096894 [TBL] [Abstract][Full Text] [Related]
46. LAMB3 mutations causing autosomal-dominant amelogenesis imperfecta. Kim JW; Seymen F; Lee KE; Ko J; Yildirim M; Tuna EB; Gencay K; Shin TJ; Kyun HK; Simmer JP; Hu JC J Dent Res; 2013 Oct; 92(10):899-904. PubMed ID: 23958762 [TBL] [Abstract][Full Text] [Related]
47. Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects. Hart TC; Hart PS; Gorry MC; Michalec MD; Ryu OH; Uygur C; Ozdemir D; Firatli S; Aren G; Firatli E J Med Genet; 2003 Dec; 40(12):900-6. PubMed ID: 14684688 [TBL] [Abstract][Full Text] [Related]
48. Novel FAM20A mutations in hypoplastic amelogenesis imperfecta. Cho SH; Seymen F; Lee KE; Lee SK; Kweon YS; Kim KJ; Jung SE; Song SJ; Yildirim M; Bayram M; Tuna EB; Gencay K; Kim JW Hum Mutat; 2012 Jan; 33(1):91-4. PubMed ID: 21990045 [TBL] [Abstract][Full Text] [Related]
49. The enamel proteins in human amelogenesis imperfecta. Wright JT; Hall KI; Yamauche M Arch Oral Biol; 1997 Feb; 42(2):149-59. PubMed ID: 9134127 [TBL] [Abstract][Full Text] [Related]
50. A novel FAM83H variant causes familial amelogenesis imperfecta with incomplete penetrance. Bai RQ; He WB; Peng Q; Shen SH; Yu QQ; Du J; Tan YQ; Wang YH; Liu BJ Mol Genet Genomic Med; 2022 Apr; 10(4):e1902. PubMed ID: 35212465 [TBL] [Abstract][Full Text] [Related]
51. Relationship of phenotype and genotype in X-linked amelogenesis imperfecta. Wright JT; Hart PS; Aldred MJ; Seow K; Crawford PJ; Hong SP; Gibson CW; Hart TC Connect Tissue Res; 2003; 44 Suppl 1():72-8. PubMed ID: 12952177 [TBL] [Abstract][Full Text] [Related]
52. Hypomaturation amelogenesis imperfecta due to WDR72 mutations: a novel mutation and ultrastructural analyses of deciduous teeth. El-Sayed W; Shore RC; Parry DA; Inglehearn CF; Mighell AJ Cells Tissues Organs; 2011; 194(1):60-6. PubMed ID: 21196691 [TBL] [Abstract][Full Text] [Related]
53. 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]
54. Enamelin and autosomal-dominant amelogenesis imperfecta. Hu JC; Yamakoshi Y Crit Rev Oral Biol Med; 2003; 14(6):387-98. PubMed ID: 14656895 [TBL] [Abstract][Full Text] [Related]
55. Mutations in RELT cause autosomal recessive amelogenesis imperfecta. Kim JW; Zhang H; Seymen F; Koruyucu M; Hu Y; Kang J; Kim YJ; Ikeda A; Kasimoglu Y; Bayram M; Zhang C; Kawasaki K; Bartlett JD; Saunders TL; Simmer JP; Hu JC Clin Genet; 2019 Mar; 95(3):375-383. PubMed ID: 30506946 [TBL] [Abstract][Full Text] [Related]
56. Novel WDR72 mutation and cytoplasmic localization. Lee SK; Seymen F; Lee KE; Kang HY; Yildirim M; Tuna EB; Gencay K; Hwang YH; Nam KH; De La Garza RJ; Hu JC; Simmer JP; Kim JW J Dent Res; 2010 Dec; 89(12):1378-82. PubMed ID: 20938048 [TBL] [Abstract][Full Text] [Related]