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Journal Abstract Search

102 related items for PubMed ID: 4516465

  • 1. Autosomal recessive pigmented hypomaturation amelogenesis imperfecta. Report of a kindred.
    Witkop CJ, Kuhlmann W, Sauk J.
    Oral Surg Oral Med Oral Pathol; 1973 Sep; 36(3):367-82. PubMed ID: 4516465
    [No Abstract] [Full Text] [Related]

  • 2. Enamel ultrastructure in pigmented hypomaturation amelogenesis imperfecta.
    Wright JT, Lord V, Robinson C, Shore R.
    J Oral Pathol Med; 1992 Oct; 21(9):390-4. PubMed ID: 1432732
    [Abstract] [Full Text] [Related]

  • 3. Analysis of a kindred with amelogenesis imperfecta.
    Wright JT.
    J Oral Pathol; 1985 May; 14(5):366-74. PubMed ID: 3925102
    [Abstract] [Full Text] [Related]

  • 4. Hypomaturation amelogenesis imperfecta caused by a novel SLC24A4 mutation.
    Herzog CR, Reid BM, Seymen F, Koruyucu M, Tuna EB, Simmer JP, Hu JC.
    Oral Surg Oral Med Oral Pathol Oral Radiol; 2015 Feb; 119(2):e77-81. PubMed ID: 25442250
    [Abstract] [Full Text] [Related]

  • 5. MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta.
    Kim JW, Simmer JP, Hart TC, Hart PS, Ramaswami MD, Bartlett JD, Hu JC.
    J Med Genet; 2005 Mar; 42(3):271-5. PubMed ID: 15744043
    [No Abstract] [Full Text] [Related]

  • 6. A clinical, genetic, and ultrastructural study of snow-capped teeth: amelogenesis imperfecta, hypomaturation type.
    Escobar VH, Goldblatt LI, Bixler D.
    Oral Surg Oral Med Oral Pathol; 1981 Dec; 52(6):607-14. PubMed ID: 6947186
    [Abstract] [Full Text] [Related]

  • 7. Amelogenesis imperfecta among Israeli Jews and the description of a new type of local hypoplastic autosomal recessive amelogenesis imperfecta.
    Chosack A, Eidelman E, Wisotski I, Cohen T.
    Oral Surg Oral Med Oral Pathol; 1979 Feb; 47(2):148-56. PubMed ID: 284277
    [Abstract] [Full Text] [Related]

  • 8. Congenital hypodontia of maxillary lateral incisors in association with coloboma of the iris and hypomaturation type of amelogenesis imperfecta in a large kindred.
    Atasu M, Eryilmaz A, Genc A, Ozcan M, Ozbayrak S.
    J Clin Pediatr Dent; 1997 Feb; 21(4):341-55. PubMed ID: 9484124
    [Abstract] [Full Text] [Related]

  • 9. Exonal deletion of SLC24A4 causes hypomaturation amelogenesis imperfecta.
    Seymen F, Lee KE, Tran Le CG, Yildirim M, Gencay K, Lee ZH, Kim JW.
    J Dent Res; 2014 Apr; 93(4):366-70. PubMed ID: 24532815
    [Abstract] [Full Text] [Related]

  • 10. Hypomaturation amelogenesis imperfecta: account of a family with an X-linked inheritance pattern.
    Bundzman ER, Modesto A.
    Braz Dent J; 1999 Apr; 10(2):111-6. PubMed ID: 10863398
    [Abstract] [Full Text] [Related]

  • 11. X-linked hypomaturation type of amelogenesis imperfecta exhibiting lyonization in affected females.
    McLarty EL, Giansanti JS, Hibbard ED.
    Oral Surg Oral Med Oral Pathol; 1973 Nov; 36(5):678-85. PubMed ID: 4518031
    [No Abstract] [Full Text] [Related]

  • 12. A kindred showing hypocalcified amelogenesis imperfecta: report of case.
    Giansanti JS.
    J Am Dent Assoc; 1973 Mar; 86(3):675-8. PubMed ID: 4510007
    [No Abstract] [Full Text] [Related]

  • 13. Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta.
    Hart PS, Hart TC, Michalec MD, Ryu OH, Simmons D, Hong S, Wright JT.
    J Med Genet; 2004 Jul; 41(7):545-9. PubMed ID: 15235027
    [No Abstract] [Full Text] [Related]

  • 14. [Observations of familial cases of amelogenesis imperfecta and a critical review].
    Bertelli E, Ferrari M, Corsi S, Berti M.
    Minerva Stomatol; 1987 Nov; 36(11):823-8. PubMed ID: 3323869
    [No Abstract] [Full Text] [Related]

  • 15. X-linked recessive hypomaturation amelogenesis imperfecta: report of case.
    Haug RH, Ferguson FS.
    J Am Dent Assoc; 1981 Jun; 102(6):865-7. PubMed ID: 6946128
    [No Abstract] [Full Text] [Related]

  • 16. Enamelin/ameloblastin gene polymorphisms in autosomal amelogenesis imperfecta among Syrian families.
    Dashash M, Bazrafshani MR, Poulton K, Jaber S, Naeem E, Blinkhorn AS.
    J Investig Clin Dent; 2011 Feb; 2(1):16-22. PubMed ID: 25427323
    [Abstract] [Full Text] [Related]

  • 17. 'Amelogenesis imperfecta: autosomal dominant hypomaturation-hypoplasia type with taurodontism'.
    Aldred MJ, Crawford PJ.
    Br Dent J; 1988 May 21; 164(10):310. PubMed ID: 3164621
    [No Abstract] [Full Text] [Related]

  • 18. MMP20 active-site mutation in hypomaturation amelogenesis imperfecta.
    Ozdemir D, Hart PS, Ryu OH, Choi SJ, Ozdemir-Karatas M, Firatli E, Piesco N, Hart TC.
    J Dent Res; 2005 Nov 21; 84(11):1031-5. PubMed ID: 16246936
    [Abstract] [Full Text] [Related]

  • 19. A progressive cone-rod dystrophy and amelogenesis imperfecta: a new syndrome.
    Jalili IK, Smith NJ.
    J Med Genet; 1988 Nov 21; 25(11):738-40. PubMed ID: 3236352
    [Abstract] [Full Text] [Related]

  • 20. Enamel ultrastructure and protein content in X-linked amelogenesis imperfecta.
    Wright JT, Aldred MJ, Crawford PJ, Kirkham J, Robinson C.
    Oral Surg Oral Med Oral Pathol; 1993 Aug 21; 76(2):192-9. PubMed ID: 8361731
    [Abstract] [Full Text] [Related]

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