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Journal Abstract Search

303 related items for PubMed ID: 27491081

  • 1. 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; 71():110-116. PubMed ID: 27491081
    [Abstract] [Full Text] [Related]

  • 2. 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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  • 3. 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; 61():144-8. PubMed ID: 26571067
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  • 4. A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.
    Abdalla EM, Mostowska A, Jagodziński PP, Dwidar K, Ismail SR.
    Arch Oral Biol; 2014 Jul; 59(7):722-8. PubMed ID: 24798981
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  • 8. 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; 97(2):155-162. PubMed ID: 28910570
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  • 10. Genes affecting tooth morphogenesis.
    Kapadia H, Mues G, D'Souza R.
    Orthod Craniofac Res; 2007 Nov; 10(4):237-44. PubMed ID: 17973693
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  • 11. Familial oligodontia and regional odontodysplasia associated with a PAX9 initiation codon mutation.
    Koskinen S, Keski-Filppula R, Alapulli H, Nieminen P, Anttonen V.
    Clin Oral Investig; 2019 Nov; 23(11):4107-4111. PubMed ID: 30809714
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  • 14. 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
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  • 15. PAX9 gene mutations and tooth agenesis: A review.
    Bonczek O, Balcar VJ, Šerý O.
    Clin Genet; 2017 Nov; 92(5):467-476. PubMed ID: 28155232
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  • 18. WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies.
    Mostowska A, Biedziak B, Zadurska M, Matuszewska-Trojan S, Jagodziński PP.
    Eur J Oral Sci; 2015 Feb; 123(1):1-8. PubMed ID: 25545742
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  • 20. 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; 120(4):278-82. PubMed ID: 22813217
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