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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

221 related items for PubMed ID: 24532815

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  • 25. Alteration of Exon Definition Causes Amelogenesis Imperfecta.
    Kim YJ, Kang J, Seymen F, Koruyucu M, Zhang H, Kasimoglu Y, Bayram M, Tuna-Ince EB, Bayrak S, Tuloglu N, Hu JC, Simmer JP, Kim JW.
    J Dent Res; 2020 Apr; 99(4):410-418. PubMed ID: 31999931
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  • 28. Hypomaturation amelogenesis imperfecta due to WDR72 mutations: a novel mutation and ultrastructural analyses of deciduous teeth.
    El-Sayed W, Shore RC, Parry DA, Inglehearn CF, Mighell AJ.
    Cells Tissues Organs; 2011 Apr; 194(1):60-6. PubMed ID: 21196691
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  • 30. Analysis of a kindred with amelogenesis imperfecta.
    Wright JT.
    J Oral Pathol; 1985 May; 14(5):366-74. PubMed ID: 3925102
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  • 31. Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1).
    Lench NJ, Winter GB.
    Hum Mutat; 1995 May; 5(3):251-9. PubMed ID: 7599636
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  • 33. 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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  • 37. WDR72 Mutations Associated with Amelogenesis Imperfecta and Acidosis.
    Zhang H, Koruyucu M, Seymen F, Kasimoglu Y, Kim JW, Tinawi S, Zhang C, Jacquemont ML, Vieira AR, Simmer JP, Hu JCC.
    J Dent Res; 2019 May; 98(5):541-548. PubMed ID: 30779877
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