These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


81 related items for PubMed ID: 5252165

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Dentin dysplasia, type II linkage to chromosome 4q.
    Dean JA, Hartsfield JK, Wright JT, Hart TC.
    J Craniofac Genet Dev Biol; 1997; 17(4):172-7. PubMed ID: 9493074
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Dentin dysplasia: endodontic considerations and report of involvement of three siblings.
    Rankow H, Miller AS.
    J Endod; 1984 Aug; 10(8):384-6. PubMed ID: 6590748
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. [Hereditary type II dentin dysplasia].
    Wetzel WE, Weckler C.
    Dtsch Zahnarztl Z; 1985 Dec; 40(12):1249-53. PubMed ID: 3869538
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Dentin dysplasia type I--a case report.
    Neumann F, Würfel F, Mundt T.
    Ann Anat; 1999 Jan; 181(1):138-40. PubMed ID: 10081578
    [Abstract] [Full Text] [Related]

  • 10. [Electron microscopic findings in hereditary dentin dysplasia].
    Koçkapan C, Wetzel WE, Hering HJ.
    Dtsch Zahnarztl Z; 1981 Jan; 36(1):60-6. PubMed ID: 6939573
    [No Abstract] [Full Text] [Related]

  • 11. Absent lamina dura associated with a developmental dentin abnormality. A family study.
    Graham WL, Harley JB, Alberico C, Kelln EE.
    Arch Intern Med; 1965 Dec; 116(6):837-41. PubMed ID: 5848215
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Dental structural diseases mapping to human chromosome 4q21.
    MacDougall M.
    Connect Tissue Res; 2003 Dec; 44 Suppl 1():285-91. PubMed ID: 12952210
    [Abstract] [Full Text] [Related]

  • 18. Dentinal dysplasia type I: review of the literature and report of a family.
    Ansari G, Reid JS.
    ASDC J Dent Child; 1997 Dec; 64(6):429-34. PubMed ID: 9466016
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. [2 cases of hereditary dentin dysplasia].
    Szpringer M, Janicha J.
    Czas Stomatol; 1974 Apr; 27(4):329-35. PubMed ID: 4207974
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 5.