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PUBMED FOR HANDHELDS

Journal Abstract Search


149 related items for PubMed ID: 9083938

  • 21. A nomenclature for X-linked amelogenesis imperfecta.
    Hart PS, Hart TC, Simmer JP, Wright JT.
    Arch Oral Biol; 2002 Apr; 47(4):255-60. PubMed ID: 11922868
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  • 29. Genes and related proteins involved in amelogenesis imperfecta.
    Stephanopoulos G, Garefalaki ME, Lyroudia K.
    J Dent Res; 2005 Dec; 84(12):1117-26. PubMed ID: 16304440
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  • 31. Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta.
    Santos MC, Hart PS, Ramaswami M, Kanno CM, Hart TC, Line SR.
    Head Face Med; 2007 Jan 31; 3():8. PubMed ID: 17266769
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  • 34. Mutational analysis of candidate genes in 24 amelogenesis imperfecta families.
    Kim JW, Simmer JP, Lin BP, Seymen F, Bartlett JD, Hu JC.
    Eur J Oral Sci; 2006 May 31; 114 Suppl 1():3-12; discussion 39-41, 379. PubMed ID: 16674655
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  • 36. 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 May 31; 7(12):e52052. PubMed ID: 23251683
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  • 38. Amelogenesis imperfecta due to a mutation of the enamelin gene: clinical case with genotype-phenotype correlations.
    Lindemeyer RG, Gibson CW, Wright TJ.
    Pediatr Dent; 2010 May 31; 32(1):56-60. PubMed ID: 20298654
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  • 39. Mutations Causing X-Linked Amelogenesis Imperfecta Alter miRNA Formation from Amelogenin Exon4.
    Shemirani R, Le MH, Nakano Y.
    J Dent Res; 2023 Oct 31; 102(11):1210-1219. PubMed ID: 37563801
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  • 40. Novel FAM20A mutation causes autosomal recessive amelogenesis imperfecta.
    Volodarsky M, Zilberman U, Birk OS.
    Arch Oral Biol; 2015 Jun 31; 60(6):919-22. PubMed ID: 25827751
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