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.
167 related articles for article (PubMed ID: 36293320)
1. Yu M; Liu H; Liu Y; Zheng J; Wu J; Sun K; Feng H; Liu H; Han D Int J Mol Sci; 2022 Oct; 23(20):. PubMed ID: 36293320 [TBL] [Abstract][Full Text] [Related]
2. Identification of a novel missense heterozygous mutation in the KDF1 gene for non-syndromic congenital anodontia. Pan Y; Yi S; Chen D; Du X; Yao X; He F; Xiong F Clin Oral Investig; 2022 Aug; 26(8):5171-5179. PubMed ID: 35641834 [TBL] [Abstract][Full Text] [Related]
3. KDF1 is a novel candidate gene of non-syndromic tooth agenesis. Zeng B; Lu H; Xiao X; Yu X; Li S; Zhu L; Yu D; Zhao W Arch Oral Biol; 2019 Jan; 97():131-136. PubMed ID: 30384154 [TBL] [Abstract][Full Text] [Related]
4. Tooth agenesis related to a novel KDF1 variant: A case report and literature review. Intarak N; Manaspon C; Theerapanon T; Prommanee S; Samaranayake L; Shotelersuk V; Porntaveetus T Oral Dis; 2024 Nov; 30(8):5195-5202. PubMed ID: 38501196 [TBL] [Abstract][Full Text] [Related]
5. Mutations in WNT10B Are Identified in Individuals with Oligodontia. Yu P; Yang W; Han D; Wang X; Guo S; Li J; Li F; Zhang X; Wong SW; Bai B; Liu Y; Du J; Sun ZS; Shi S; Feng H; Cai T Am J Hum Genet; 2016 Jul; 99(1):195-201. PubMed ID: 27321946 [TBL] [Abstract][Full Text] [Related]
6. Whole exome sequencing in an Italian family with isolated maxillary canine agenesis and canine eruption anomalies. Barbato E; Traversa A; Guarnieri R; Giovannetti A; Genovesi ML; Magliozzi MR; Paolacci S; Ciolfi A; Pizzi S; Di Giorgio R; Tartaglia M; Pizzuti A; Caputo V Arch Oral Biol; 2018 Jul; 91():96-102. PubMed ID: 29705498 [TBL] [Abstract][Full Text] [Related]
7. Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis. Dinckan N; Du R; Petty LE; Coban-Akdemir Z; Jhangiani SN; Paine I; Baugh EH; Erdem AP; Kayserili H; Doddapaneni H; Hu J; Muzny DM; Boerwinkle E; Gibbs RA; Lupski JR; Uyguner ZO; Below JE; Letra A J Dent Res; 2018 Jan; 97(1):49-59. PubMed ID: 28813618 [TBL] [Abstract][Full Text] [Related]
8. Expanding the genetic spectrum of tooth agenesis using whole-exome sequencing. Yu K; Dou J; Huang W; Wang F; Wu Y Clin Genet; 2022 Dec; 102(6):503-516. PubMed ID: 36071541 [TBL] [Abstract][Full Text] [Related]
9. Four Novel Liu H; Liu H; Su L; Zheng J; Feng H; Liu Y; Yu M; Han D Int J Mol Sci; 2022 Jul; 23(15):. PubMed ID: 35897718 [TBL] [Abstract][Full Text] [Related]
10. Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis. Mostowska A; Biedziak B; Zadurska M; Dunin-Wilczynska I; Lianeri M; Jagodzinski PP Clin Genet; 2013 Nov; 84(5):429-40. PubMed ID: 23167694 [TBL] [Abstract][Full Text] [Related]
11. Yu M; Fan Z; Wong SW; Sun K; Zhang L; Liu H; Feng H; Liu Y; Han D J Dent Res; 2021 Apr; 100(4):415-422. PubMed ID: 33164649 [TBL] [Abstract][Full Text] [Related]
12. Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis. Salvi A; Giacopuzzi E; Bardellini E; Amadori F; Ferrari L; De Petro G; Borsani G; Majorana A Int J Mol Med; 2016 Nov; 38(5):1338-1348. PubMed ID: 27665865 [TBL] [Abstract][Full Text] [Related]
13. Agenesis of maxillary lateral incisors and associated dental anomalies. Garib DG; Alencar BM; Lauris JR; Baccetti T Am J Orthod Dentofacial Orthop; 2010 Jun; 137(6):732.e1-6; discussion 732-3. PubMed ID: 20685523 [TBL] [Abstract][Full Text] [Related]
15. Enamel Structure Defects in Li P; Zeng B; Xie W; Xiao X; Lin L; Yu D; Zhao W Biomedicines; 2023 Feb; 11(2):. PubMed ID: 36831017 [TBL] [Abstract][Full Text] [Related]
16. A novel missense mutation of LRP6 identified by whole-exome sequencing in a Chinese family with non-syndromic tooth agenesis. Wang H; Liu Y; Zheng Y; Zhao X; Lin S; Zhang Q; Zhang X Orthod Craniofac Res; 2021 May; 24(2):233-240. PubMed ID: 32844563 [TBL] [Abstract][Full Text] [Related]
17. Novel mutations identified in patients with tooth agenesis by whole-exome sequencing. Zhao K; Lian M; Zou D; Huang W; Zhou W; Shen Y; Wang F; Wu Y Oral Dis; 2019 Mar; 25(2):523-534. PubMed ID: 30417976 [TBL] [Abstract][Full Text] [Related]
18. A novel EDAR missense mutation identified by whole-exome sequencing with non-syndromic tooth agenesis in a Chinese family. Zhang H; Kong X; Ren J; Yuan S; Liu C; Hou Y; Liu Y; Meng L; Zhang G; Du Q; Shen W Mol Genet Genomic Med; 2021 Jun; 9(6):e1684. PubMed ID: 33943035 [TBL] [Abstract][Full Text] [Related]
19. Characterization of novel MSX1 variants causally associated with non-syndromic oligodontia in Chinese families. Zhao Y; Ren J; Meng L; Hou Y; Liu C; Zhang G; Shen W Mol Genet Genomic Med; 2024 Jan; 12(1):e2334. PubMed ID: 38069551 [TBL] [Abstract][Full Text] [Related]
20. Novel PITX2 mutations identified in Axenfeld-Rieger syndrome and the pattern of PITX2-related tooth agenesis. Fan Z; Sun S; Liu H; Yu M; Liu Z; Wong SW; Liu Y; Han D; Feng H Oral Dis; 2019 Nov; 25(8):2010-2019. PubMed ID: 31529555 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]