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Journal Abstract Search


309 related items for PubMed ID: 30799455

  • 1. [Alteración del gen AMELX en amelogénesis imperfecta. Una breve revisión].
    Tremillo-Maldonado O, Molina-Frechero N, González-González R, Bologna-Molina R.
    Gac Med Mex; 2019; 155(1):101-107. PubMed ID: 30799455
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  • 2. Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutations.
    Hart PS, Aldred MJ, Crawford PJ, Wright NJ, Hart TC, Wright JT.
    Arch Oral Biol; 2002 Apr; 47(4):261-5. PubMed ID: 11922869
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  • 4. Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6.
    Hu JC, Chan HC, Simmer SG, Seymen F, Richardson AS, Hu Y, Milkovich RN, Estrella NM, Yildirim M, Bayram M, Chen CF, Simmer JP.
    PLoS One; 2012 Apr; 7(12):e52052. PubMed ID: 23251683
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  • 6. Relationship of phenotype and genotype in X-linked amelogenesis imperfecta.
    Wright JT, Hart PS, Aldred MJ, Seow K, Crawford PJ, Hong SP, Gibson CW, Hart TC.
    Connect Tissue Res; 2003 Apr; 44 Suppl 1():72-8. PubMed ID: 12952177
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  • 8. Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutation.
    Ravassipour DB, Hart PS, Hart TC, Ritter AV, Yamauchi M, Gibson C, Wright JT.
    J Dent Res; 2000 Jul; 79(7):1476-81. PubMed ID: 11005731
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  • 14. Alteration of conserved alternative splicing in AMELX causes enamel defects.
    Cho ES, Kim KJ, Lee KE, Lee EJ, Yun CY, Lee MJ, Shin TJ, Hyun HK, Kim YJ, Lee SH, Jung HS, Lee ZH, Kim JW.
    J Dent Res; 2014 Oct; 93(10):980-7. PubMed ID: 25117480
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