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207 related items for PubMed ID: 24316698
1. Exclusion of PAX9 and MSX1 mutation in six families affected by tooth agenesis. A genetic study and literature review. Tallón-Walton V, Manzanares-Céspedes MC, Carvalho-Lobato P, Valdivia-Gandur I, Arte S, Nieminen P. Med Oral Patol Oral Cir Bucal; 2014 May 01; 19(3):e248-54. PubMed ID: 24316698 [Abstract] [Full Text] [Related]
2. Nine Novel PAX9 Mutations and a Distinct Tooth Agenesis Genotype-Phenotype. Wong SW, Han D, Zhang H, Liu Y, Zhang X, Miao MZ, Wang Y, Zhao N, Zeng L, Bai B, Wang YX, Liu H, Frazier-Bowers SA, Feng H. J Dent Res; 2018 Feb 01; 97(2):155-162. PubMed ID: 28910570 [Abstract] [Full Text] [Related]
3. Mutations in MSX1, PAX9 and MMP20 genes in Saudi Arabian patients with tooth agenesis. Shahid M, Balto HA, Al-Hammad N, Joshi S, Khalil HS, Somily AM, Sinjilawi NA, Al-Ghamdi S, Faiyaz-Ul-Haque M, Dhillon VS. Eur J Med Genet; 2016 Aug 01; 59(8):377-85. PubMed ID: 27365112 [Abstract] [Full Text] [Related]
4. [Correlation between the phenotype and genotype of tooth agenesis patients by tooth agenesis code]. Gong Y, Feng HL, He HY, Ge YJ. Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2010 Jun 01; 32(3):254-9. PubMed ID: 20602873 [Abstract] [Full Text] [Related]
5. Msx1 mutations: how do they cause tooth agenesis? Wang Y, Kong H, Mues G, D'Souza R. J Dent Res; 2011 Mar 01; 90(3):311-6. PubMed ID: 21297014 [Abstract] [Full Text] [Related]
6. Associations between the risk of tooth agenesis and single-nucleotide polymorphisms of MSX1 and PAX9 genes in nonsyndromic cleft patients. Seo YJ, Park JW, Kim YH, Baek SH. Angle Orthod; 2013 Nov 01; 83(6):1036-42. PubMed ID: 23718693 [Abstract] [Full Text] [Related]
8. PAX9 polymorphism and susceptibility to sporadic non-syndromic severe anodontia: a case-control study in southwest China. Wang J, Xu Y, Chen J, Wang F, Huang R, Wu S, Shu L, Qiu J, Yang Z, Xue J, Wang R, Zhao J, Lai W. J Appl Oral Sci; 2013 Aug 01; 21(3):256-64. PubMed ID: 23857653 [Abstract] [Full Text] [Related]
9. Exclusion of coding region mutations in MSX1, PAX9 and AXIN2 in eight patients with severe oligodontia phenotype. Gerits A, Nieminen P, De Muynck S, Carels C. Orthod Craniofac Res; 2006 Aug 01; 9(3):129-36. PubMed ID: 16918677 [Abstract] [Full Text] [Related]
11. 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 01; 38(5):1338-1348. PubMed ID: 27665865 [Abstract] [Full Text] [Related]
12. Effects of PAX9 and MSX1 gene variants to hypodontia, tooth size and the type of congenitally missing teeth. Kirac D, Eraydin F, Avcilar T, Ulucan K, Özdemir F, Guney AI, Kaspar EÇ, Keshi E, Isbir T. Cell Mol Biol (Noisy-le-grand); 2016 Nov 30; 62(13):78-84. PubMed ID: 28040065 [Abstract] [Full Text] [Related]
14. MSX1 and PAX9 investigation in monozygotic twins with variable expression of tooth agenesis. Lopez SI, Mundstock KS, Paixão-Côrtes VR, Schüler-Faccini L, Mundstock CA, Bortolini MC, Salzano FM. Twin Res Hum Genet; 2013 Dec 30; 16(6):1112-6. PubMed ID: 24103583 [Abstract] [Full Text] [Related]
15. Mutational analysis of MSX1 and PAX9 genes in Portuguese families with maxillary lateral incisor agenesis. Pinho T, Silva-Fernandes A, Bousbaa H, Maciel P. Eur J Orthod; 2010 Oct 30; 32(5):582-8. PubMed ID: 20660504 [Abstract] [Full Text] [Related]
16. Novel nonsense mutation in MSX1 causes tooth agenesis with cleft lip in a Chinese family. Liang J, Zhu L, Meng L, Chen D, Bian Z. Eur J Oral Sci; 2012 Aug 30; 120(4):278-82. PubMed ID: 22813217 [Abstract] [Full Text] [Related]
17. Characterization of a novel mutation in PAX9 gene in a family with non-syndromic dental agenesis. Haddaji Mastouri M, De Coster P, Zaghabani A, Trabelsi S, May Y, Saad A, Coucke P, H'mida Ben Brahim D. Arch Oral Biol; 2016 Nov 30; 71():110-116. PubMed ID: 27491081 [Abstract] [Full Text] [Related]
18. Novel MSX1 frameshift causes autosomal-dominant oligodontia. Kim JW, Simmer JP, Lin BP, Hu JC. J Dent Res; 2006 Mar 30; 85(3):267-71. PubMed ID: 16498076 [Abstract] [Full Text] [Related]
19. A novel initiation codon mutation of PAX9 in a family with oligodontia. Liang J, Qin C, Yue H, He H, Bian Z. Arch Oral Biol; 2016 Jan 30; 61():144-8. PubMed ID: 26571067 [Abstract] [Full Text] [Related]
20. Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes. Bergendal B, Klar J, Stecksén-Blicks C, Norderyd J, Dahl N. Am J Med Genet A; 2011 Jul 30; 155A(7):1616-22. PubMed ID: 21626677 [Abstract] [Full Text] [Related] Page: [Next] [New Search]