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Journal Abstract Search

164 related items for PubMed ID: 6591174

  • 1. The treatment of hypoplastic and hypomineralised teeth.
    Andlaw RJ.
    Proc Br Paedod Soc; 1983; 13():25-30. PubMed ID: 6591174
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  • 3. Diagnosis of enamel defects.
    Sarnat H, Moss SJ.
    N Y State Dent J; 1985 Feb; 51(2):103-4, 106. PubMed ID: 3856783
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  • 6. Amelogenesis imperfecta: a clinician's challenge.
    Chamarthi V, Varma BR, Jayanthi M.
    J Indian Soc Pedod Prev Dent; 2012 Feb; 30(1):70-3. PubMed ID: 22565521
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  • 7. [Amelogenesis imperfecta in young patients].
    Roeters FJ, Frankenmolen FW.
    Ned Tijdschr Tandheelkd; 1997 Feb; 104(2):78-80. PubMed ID: 11924374
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  • 9. [Genetic defects of the enamel].
    Skrinjarić I.
    Acta Stomatol Croat; 1985 Feb; 19(1):57-67. PubMed ID: 3859996
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  • 12. ENAM mutations in autosomal-dominant amelogenesis imperfecta.
    Kim JW, Seymen F, Lin BP, Kiziltan B, Gencay K, Simmer JP, Hu JC.
    J Dent Res; 2005 Mar; 84(3):278-82. PubMed ID: 15723871
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  • 14. [Apparently hereditary hypocalcification enamel anomaly].
    Jolán B.
    Fogorv Sz; 1970 Jun; 63(6):170-3. PubMed ID: 5270198
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  • 15. Developmental Defects of Enamel.
    Martins DDS, Ionta FQ, Pompermaier Garlet G, Lima RR, Neves AA, Rios D, Lussi A.
    Monogr Oral Sci; 2024 Jun; 32():10-34. PubMed ID: 39321764
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  • 16. Hypoplastic-hypomaturation amelogenesis imperfecta with taurodontism: report of case.
    Parker JL, Regattieri LR, Thomas JP.
    ASDC J Dent Child; 1975 Jun; 42(5):379-83. PubMed ID: 1100695
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  • 17. A new classification of heritable human enamel defects and a discussion of dentin defects.
    Shields ED.
    Birth Defects Orig Artic Ser; 1983 Jun; 19(1):107-27. PubMed ID: 6362739
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  • 18. [Diagnosis and treatment of developmental defects of enamel and dentin in young children].
    Sapir S.
    Refuat Hapeh Vehashinayim (1993); 2005 Jul; 22(3):60-74, 91. PubMed ID: 16323410
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  • 19. Craniofacial structure related to inheritance pattern in amelogenesis imperfecta.
    Bäckman B, Adolfsson U.
    Am J Orthod Dentofacial Orthop; 1994 Jun; 105(6):575-82. PubMed ID: 8198082
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  • 20. Amelogenesis imperfecta: autosomal dominant hypomaturation-hypoplasia type with taurodontism.
    Crawford PJ, Evans RD, Aldred MJ.
    Br Dent J; 1988 Feb 06; 164(3):71-3. PubMed ID: 3422811
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