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.
23. Novel FAM83H mutations in patients with amelogenesis imperfecta. Xin W; Wenjun W; Man Q; Yuming Z Sci Rep; 2017 Jul; 7(1):6075. PubMed ID: 28729668 [TBL] [Abstract][Full Text] [Related]
24. Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta. El-Sayed W; Parry DA; Shore RC; Ahmed M; Jafri H; Rashid Y; Al-Bahlani S; Al Harasi S; Kirkham J; Inglehearn CF; Mighell AJ Am J Hum Genet; 2009 Nov; 85(5):699-705. PubMed ID: 19853237 [TBL] [Abstract][Full Text] [Related]
25. Novel ENAM and LAMB3 mutations in Chinese families with hypoplastic amelogenesis imperfecta. Wang X; Zhao Y; Yang Y; Qin M PLoS One; 2015; 10(3):e0116514. PubMed ID: 25769099 [TBL] [Abstract][Full Text] [Related]
26. Localization of a gene for autosomal dominant amelogenesis imperfecta (ADAI) to chromosome 4q. Forsman K; Lind L; Bäckman B; Westermark E; Holmgren G Hum Mol Genet; 1994 Sep; 3(9):1621-5. PubMed ID: 7833920 [TBL] [Abstract][Full Text] [Related]
27. Amelogenesis imperfecta among Israeli Jews and the description of a new type of local hypoplastic autosomal recessive amelogenesis imperfecta. Chosack A; Eidelman E; Wisotski I; Cohen T Oral Surg Oral Med Oral Pathol; 1979 Feb; 47(2):148-56. PubMed ID: 284277 [TBL] [Abstract][Full Text] [Related]
28. Wang SK; Zhang H; Hu CY; Liu JF; Chadha S; Kim JW; Simmer JP; Hu JCC J Dent Res; 2021 Mar; 100(3):293-301. PubMed ID: 33034243 [TBL] [Abstract][Full Text] [Related]
29. The mineral composition and enamel ultrastructure of hypocalcified amelogenesis imperfecta. Wright JT; Duggal MS; Robinson C; Kirkham J; Shore R J Craniofac Genet Dev Biol; 1993; 13(2):117-26. PubMed ID: 8325967 [TBL] [Abstract][Full Text] [Related]
30. Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary. Kida M; Ariga T; Shirakawa T; Oguchi H; Sakiyama Y J Dent Res; 2002 Nov; 81(11):738-42. PubMed ID: 12407086 [TBL] [Abstract][Full Text] [Related]
31. Ultrastructural analysis of the teeth affected by amelogenesis imperfecta resulting from FAM83H mutations and review of the literature. Zhang C; Song Y; Bian Z Oral Surg Oral Med Oral Pathol Oral Radiol; 2015 Feb; 119(2):e69-76. PubMed ID: 25487982 [TBL] [Abstract][Full Text] [Related]
32. A novel FAM83H mutation in one Chinese family with autosomal-dominant hypocalcification amelogenesis imperfecta. Yu S; Quan J; Wang X; Sun X; Zhang X; Liu Y; Zhang C; Zheng S Mutagenesis; 2018 Oct; 33(4):333-340. PubMed ID: 30247735 [TBL] [Abstract][Full Text] [Related]
33. Amelogenesis imperfecta in a Chinese family resulting from a FAM83H variation and the effect of FAM83H on the secretion of enamel matrix proteins. Xie Y; Meng M; Cao L; Yang J; Ma Q; Huang X; Yu Y; Yang Q; Zou J; Du Q Clin Oral Investig; 2023 Mar; 27(3):1289-1299. PubMed ID: 36318336 [TBL] [Abstract][Full Text] [Related]
34. [Analysis of amelogenesis imperfecta with abnormal tooth eruption caused by FAM83H mutation]. Mao SY; Duan XH Zhonghua Kou Qiang Yi Xue Za Zhi; 2023 Sep; 58(9):933-937. PubMed ID: 37659852 [No Abstract] [Full Text] [Related]
35. A Recurrent Alvarez C; Aragón MA; Lee Y; Gutiérrez S; Méndez P; García DA; Otero L; Kim JW Children (Basel); 2022 Mar; 9(3):. PubMed ID: 35327733 [TBL] [Abstract][Full Text] [Related]
36. Effects of Fam83h truncation mutation on enamel developmental defects in male C57/BL6J mice. Zheng X; Huang W; He Z; Li Y; Li S; Song Y Bone; 2023 Jan; 166():116595. PubMed ID: 36272714 [TBL] [Abstract][Full Text] [Related]
39. Phenotypic diversity and revision of the nomenclature for autosomal recessive amelogenesis imperfecta. Nusier M; Yassin O; Hart TC; Samimi A; Wright JT Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2004 Feb; 97(2):220-30. PubMed ID: 14970781 [TBL] [Abstract][Full Text] [Related]
40. Evolutionary analysis of FAM83H in vertebrates. Huang W; Yang M; Wang C; Song Y PLoS One; 2017; 12(7):e0180360. PubMed ID: 28683132 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]