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Journal Abstract Search

222 related items for PubMed ID: 25203534

  • 21. [EDA mutation screening and phenotype analysis in patients with tooth agenesis].
    He HY, Liu Y, Han D, Liu HC, Bai BJ, Feng HL.
    Beijing Da Xue Xue Bao Yi Xue Ban; 2016 Aug 18; 48(4):686-691. PubMed ID: 29263514
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  • 22. Non-syndromic tooth agenesis in two Chinese families associated with novel missense mutations in the TNF domain of EDA (ectodysplasin A).
    Li S, Li J, Cheng J, Zhou B, Tong X, Dong X, Wang Z, Hu Q, Chen M, Hua ZC.
    PLoS One; 2008 Jun 11; 3(6):e2396. PubMed ID: 18545687
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  • 24. 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 11; 25(2):523-534. PubMed ID: 30417976
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  • 28. Functional analysis of a novel missense mutation in AXIN2 associated with non-syndromic tooth agenesis.
    Yue H, Liang J, Yang K, Hua B, Bian Z.
    Eur J Oral Sci; 2016 Jun 11; 124(3):228-33. PubMed ID: 27090353
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  • 29. EDA gene mutations underlie non-syndromic oligodontia.
    Song S, Han D, Qu H, Gong Y, Wu H, Zhang X, Zhong N, Feng H.
    J Dent Res; 2009 Feb 11; 88(2):126-31. PubMed ID: 19278982
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  • 30. A novel missense mutation in the EDA gene associated with X-linked recessive isolated hypodontia.
    Rasool M, Schuster J, Aslam M, Tariq M, Ahmad I, Ali A, Entesarian M, Dahl N, Baig SM.
    J Hum Genet; 2008 Feb 11; 53(10):894-898. PubMed ID: 18688569
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  • 32. Eight EDA mutations in Chinese patients with tooth agenesis and genotype-phenotype analysis.
    Yu K, Sheng Y, Wang F, Yang S, Wan F, Lei M, Wu Y.
    Oral Dis; 2024 Oct 11; 30(7):4598-4607. PubMed ID: 38287639
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  • 33. Genetic analysis: Wnt and other pathways in nonsyndromic tooth agenesis.
    Yu M, Wong SW, Han D, Cai T.
    Oral Dis; 2019 Apr 11; 25(3):646-651. PubMed ID: 29969831
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  • 34. [Detection of EDA gene mutation and phenotypic analysis in patients with hypohidrotic ectodermal dysplasia].
    Wu JY, Yu M, Sun SC, Fan ZZ, Zheng JL, Zhang LT, Feng HL, Liu Y, Han D.
    Beijing Da Xue Xue Bao Yi Xue Ban; 2020 Dec 09; 53(1):24-33. PubMed ID: 33550332
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  • 36. Two Novel Mutations in Ectodysplasin-A Identified in Syndromic Tooth Agenesis.
    Xie W, Zeng B, Li P, Xu D, Yu D, Zhao W.
    J Coll Physicians Surg Pak; 2022 May 09; 32(5):570-574. PubMed ID: 35546689
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  • 37. An in vitro and computational validation of a novel loss-of-functional mutation in PAX9 associated with non-syndromic tooth agenesis.
    Sarkar T, Ranjan P, Kanathur S, Gupta A, Das P.
    Mol Genet Genomics; 2023 Jan 09; 298(1):183-199. PubMed ID: 36374296
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