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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

272 related items for PubMed ID: 10863398

  • 21.
    ; . PubMed ID:
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  • 22. Clinical features of a family with X-linked amelogenesis imperfecta mapping to a new locus (AIH3) on the long arm of the X chromosome.
    Crawford PJ, Aldred MJ.
    Oral Surg Oral Med Oral Pathol; 1993 Aug; 76(2):187-91. PubMed ID: 8361730
    [Abstract] [Full Text] [Related]

  • 23. Relationship of phenotype and genotype in X-linked amelogenesis imperfecta.
    Wright JT, Hart PS, Aldred MJ, Seow K, Crawford PJ, Hong SP, Gibson CW, Hart TC.
    Connect Tissue Res; 2003 Aug; 44 Suppl 1():72-8. PubMed ID: 12952177
    [Abstract] [Full Text] [Related]

  • 24. Dental management of amelogenesis imperfecta patients: a primer on genotype-phenotype correlations.
    Ng FK, Messer LB.
    Pediatr Dent; 2009 Aug; 31(1):20-30. PubMed ID: 19320256
    [Abstract] [Full Text] [Related]

  • 25. Expanding the phenotype of hypomaturation amelogenesis imperfecta due to a novel SLC24A4 variant.
    Lepperdinger U, Maurer E, Witsch-Baumgartner M, Stigler R, Zschocke J, Lussi A, Kapferer-Seebacher I.
    Clin Oral Investig; 2020 Oct; 24(10):3519-3525. PubMed ID: 32034543
    [Abstract] [Full Text] [Related]

  • 26. 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]

  • 27.
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  • 28.
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  • 29. [Clinical report on a case of amelogenesis imperfecta].
    Yoshida T, Minegishi H, Osaka N, Irie E, Kurihara J, Goto H.
    Josai Shika Daigaku Kiyo; 1981 Dec; 10(2):315-21. PubMed ID: 6959664
    [No Abstract] [Full Text] [Related]

  • 30. Amelogenesis imperfecta: a genetic study.
    Bäckman B, Holmgren G.
    Hum Hered; 1988 Dec; 38(4):189-206. PubMed ID: 3169793
    [Abstract] [Full Text] [Related]

  • 31.
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  • 32. Molecular biology of hereditary enamel defects.
    Aldred MJ, Crawford PJ.
    Ciba Found Symp; 1997 Dec; 205():200-5; discussion 205-9. PubMed ID: 9189626
    [Abstract] [Full Text] [Related]

  • 33. Inheritance pattern and elemental composition of enamel affected by hypomaturation amelogenesis imperfecta.
    Shore RC, Bäckman B, Brookes SJ, Kirkham J, Wood SR, Robinson C.
    Connect Tissue Res; 2002 Dec; 43(2-3):466-71. PubMed ID: 12489199
    [Abstract] [Full Text] [Related]

  • 34. X-linked amelogenesis imperfecta. Presentation of two kindreds and a review of the literature.
    Crawford PJ, Aldred MJ.
    Oral Surg Oral Med Oral Pathol; 1992 Apr; 73(4):449-55. PubMed ID: 1574307
    [Abstract] [Full Text] [Related]

  • 35. Localization of a gene for autosomal dominant amelogenesis imperfecta (ADAI) to chromosome 4q.
    Forsman K, Lind L, Bäckman B, Westermark E, Holmgren G.
    Hum Mol Genet; 1994 Sep; 3(9):1621-5. PubMed ID: 7833920
    [Abstract] [Full Text] [Related]

  • 36.
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  • 37. 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]

  • 38.
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  • 39. [A contribution to hereditary amelogonesis imperfecta].
    Harzer W.
    Stomatol DDR; 1980 Jan; 30(1):41-3. PubMed ID: 6932113
    [Abstract] [Full Text] [Related]

  • 40. Clinical diagnosis and management strategies of amelogenesis imperfectavariants.
    Seow WK.
    Pediatr Dent; 1993 Jan; 15(6):384-93. PubMed ID: 8152999
    [Abstract] [Full Text] [Related]

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