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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

174 related items for PubMed ID: 23638899

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  • 3. The structure and composition of deciduous enamel affected by local hypoplastic autosomal dominant amelogenesis imperfecta resulting from an ENAM mutation.
    Shore RC, Bäckman B, Elcock C, Brook AH, Brookes SJ, Kirkham J.
    Cells Tissues Organs; 2010; 191(4):301-6. PubMed ID: 19923784
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  • 6. Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects.
    Hart TC, Hart PS, Gorry MC, Michalec MD, Ryu OH, Uygur C, Ozdemir D, Firatli S, Aren G, Firatli E.
    J Med Genet; 2003 Dec; 40(12):900-6. PubMed ID: 14684688
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  • 7. Candidate gene strategy reveals ENAM mutations.
    Kang HY, Seymen F, Lee SK, Yildirim M, Tuna EB, Patir A, Lee KE, Kim JW.
    J Dent Res; 2009 Mar; 88(3):266-9. PubMed ID: 19329462
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  • 9. An autosomal recessive mutation in SCL24A4 causing enamel hypoplasia in Samoyed and its relationship to breed-wide genetic diversity.
    Pedersen NC, Shope B, Liu H.
    Canine Genet Epidemiol; 2017 Mar; 4():11. PubMed ID: 29201383
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  • 10. Identification of the enamelin (g.8344delG) mutation in a new kindred and presentation of a standardized ENAM nomenclature.
    Hart PS, Michalec MD, Seow WK, Hart TC, Wright JT.
    Arch Oral Biol; 2003 Aug; 48(8):589-96. PubMed ID: 12828988
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  • 12. A multidisciplinary approach for the diagnosis of hypocalcified amelogenesis imperfecta in two Chilean families.
    Urzúa B, Ortega-Pinto A, Farias DA, Franco E, Morales-Bozo I, Moncada G, Escobar-Pezoa N, Scholz U, Cifuentes V.
    Acta Odontol Scand; 2012 Jan; 70(1):7-14. PubMed ID: 21504268
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  • 16. Phenotype of ENAM mutations is dosage-dependent.
    Ozdemir D, Hart PS, Firatli E, Aren G, Ryu OH, Hart TC.
    J Dent Res; 2005 Nov; 84(11):1036-41. PubMed ID: 16246937
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  • 17. Enamel defects in standard poodle dogs in Sweden.
    Mannerfelt T, Lindgren I.
    J Vet Dent; 2009 Nov; 26(4):213-5. PubMed ID: 20192019
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  • 18. Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary.
    Kida M, Ariga T, Shirakawa T, Oguchi H, Sakiyama Y.
    J Dent Res; 2002 Nov; 81(11):738-42. PubMed ID: 12407086
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