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PUBMED FOR HANDHELDS

Journal Abstract Search

145 related items for PubMed ID: 25377791

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  • 22. Genetic background of nonsyndromic oligodontia: a systematic review and meta-analysis.
    Ruf S, Klimas D, Hönemann M, Jabir S.
    J Orofac Orthop; 2013 Jul; 74(4):295-308. PubMed ID: 23828301
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  • 24. Novel mutation of the initiation codon of PAX9 causes oligodontia.
    Klein ML, Nieminen P, Lammi L, Niebuhr E, Kreiborg S.
    J Dent Res; 2005 Jan; 84(1):43-7. PubMed ID: 15615874
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  • 28. Novel PAX9 mutation associated with syndromic tooth agenesis.
    Mostowska A, Zadurska M, Rakowska A, Lianeri M, Jagodziński PP.
    Eur J Oral Sci; 2013 Oct; 121(5):403-11. PubMed ID: 24028587
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  • 32. Two novel mutations in MSX1 causing oligodontia.
    Yang L, Liang J, Yue H, Bian Z.
    PLoS One; 2020 Oct; 15(1):e0227287. PubMed ID: 31914153
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  • 33. Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene.
    Beard C, Purvis R, Winship IM, Macrae FA, Buchanan DD.
    Fam Cancer; 2019 Jul; 18(3):311-315. PubMed ID: 30671715
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  • 34. A missense mutation in PAX9 in a family with distinct phenotype of oligodontia.
    Lammi L, Halonen K, Pirinen S, Thesleff I, Arte S, Nieminen P.
    Eur J Hum Genet; 2003 Nov; 11(11):866-71. PubMed ID: 14571272
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  • 36. Identification of a novel missense mutation of MSX1 gene in Chinese family with autosomal-dominant oligodontia.
    Xuan K, Jin F, Liu YL, Yuan LT, Wen LY, Yang FS, Wang XJ, Wang GH, Jin Y.
    Arch Oral Biol; 2008 Aug; 53(8):773-9. PubMed ID: 18374898
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  • 37. Novel missense mutation in the EDA gene in a family affected by oligodontia.
    Ruiz-Heiland G, Jabir S, Wende W, Blecher S, Bock N, Ruf S.
    J Orofac Orthop; 2016 Jan; 77(1):31-8. PubMed ID: 26753551
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