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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

79 related articles for article (PubMed ID: 3523848)

  • 21. Candidate gene strategy reveals ENAM mutations.
    Kang HY; Seymen F; Lee SK; Yildirim M; Tuna EB; Patir A; Lee KE; Kim JW
    J Dent Res; 2009 Mar; 88(3):266-9. PubMed ID: 19329462
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Congenital adrenal hyperplasia and enamel hypoplasia: case report.
    Hallett KB; Hall RK
    Pediatr Dent; 1995; 17(1):54-9. PubMed ID: 7899104
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Diagnosis of enamel defects.
    Sarnat H; Moss SJ
    N Y State Dent J; 1985 Feb; 51(2):103-4, 106. PubMed ID: 3856783
    [No Abstract]   [Full Text] [Related]  

  • 24. [Problem and methodology in human genetics research in the scope of orthodontics--II].
    Schulze C
    Dtsch Zahnarztl Z; 1973 Apr; 28(4):474-80 contd. PubMed ID: 4513087
    [No Abstract]   [Full Text] [Related]  

  • 25. Identification of a novel FAM83H mutation and microhardness of an affected molar in autosomal dominant hypocalcified amelogenesis imperfecta.
    Hyun HK; Lee SK; Lee KE; Kang HY; Kim EJ; Choung PH; Kim JW
    Int Endod J; 2009 Nov; 42(11):1039-43. PubMed ID: 19825039
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The treatment of hypoplastic and hypomineralised teeth.
    Andlaw RJ
    Proc Br Paedod Soc; 1983; 13():25-30. PubMed ID: 6591174
    [No Abstract]   [Full Text] [Related]  

  • 27. [Problem solving in endodontic diseases: I. Enamel developmental defects: clinical classification and molecular biologic mechanism].
    Gao XJ; Lü P; Zhuang H
    Zhonghua Kou Qiang Yi Xue Za Zhi; 2009 May; 44(5):314-7. PubMed ID: 19575995
    [No Abstract]   [Full Text] [Related]  

  • 28. [Dental diseases and heredity].
    Nakata M
    Nihon Shika Ishikai Zasshi; 1980; 33(9):951-9. PubMed ID: 6943221
    [No Abstract]   [Full Text] [Related]  

  • 29. [A case of systemic hypomineralization of the enamel].
    Hanzély B
    Fogorv Sz; 1971 May; 64(5):150-3. PubMed ID: 5280926
    [No Abstract]   [Full Text] [Related]  

  • 30. [Genetic defects of the enamel].
    Skrinjarić I
    Acta Stomatol Croat; 1985; 19(1):57-67. PubMed ID: 3859996
    [No Abstract]   [Full Text] [Related]  

  • 31. Amelogenesis imperfecta: diagnosis and resolution of a case with hypoplasia and hypocalcification of enamel, dental agenesis, and skeletal open bite.
    Pulgar Encinas R; García-Espona I; Navajas Rodriguez de Mondelo JM
    Quintessence Int; 2001 Mar; 32(3):183-9. PubMed ID: 12066657
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Enamel hypoplasia in the primary dentition: a review.
    Seow WK
    ASDC J Dent Child; 1991; 58(6):441-52. PubMed ID: 1783694
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Dental enamel hypoplasia and open bite as autosomal dominant genetic symptoms].
    Erpenstein H; Wannenmacher E
    Dtsch Zahnarztl Z; 1968 Mar; 23(3):405-14. PubMed ID: 5240600
    [No Abstract]   [Full Text] [Related]  

  • 34. Defects in permanent teeth following pulp exposure of primary teeth.
    Binns WH; Escobar A
    J Dent Child; 1967 Jan; 34(1):4-14. PubMed ID: 5334667
    [No Abstract]   [Full Text] [Related]  

  • 35. Hereditary enamel hypoplasia: its association with characteristic hair structure.
    Robinson GC; Miller JR
    Pediatrics; 1966 Mar; 37(3):498-502. PubMed ID: 5906373
    [No Abstract]   [Full Text] [Related]  

  • 36. [Electron microscopic studies of hereditary enamel hypoplasia observed in 2 families].
    Höhling HJ; Erpenstein H
    Dtsch Zahnarztl Z; 1967 Mar; 22(3):501-13. PubMed ID: 5227147
    [No Abstract]   [Full Text] [Related]  

  • 37. Oculodentodigital dysplasia: study of ophthalmological and clinical manifestations in three boys with probably autosomal recessive inheritance.
    Frasson M; Calixto N; Cronemberger S; de Aguiar RA; Leão LL; de Aguiar MJ
    Ophthalmic Genet; 2004 Sep; 25(3):227-36. PubMed ID: 15512999
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A new classification of heritable human enamel defects and a discussion of dentin defects.
    Shields ED
    Birth Defects Orig Artic Ser; 1983; 19(1):107-27. PubMed ID: 6362739
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Recent findings on amelogenesis and mineralization of dental enamel].
    Morabito A; Defabianis P
    Minerva Stomatol; 1989 Jan; 38(1):147-9. PubMed ID: 2651869
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Hereditary enamel and dentin hypoplasia].
    Vossmerbaümer R
    Zahnarztl Prax; 1976 Mar; 27(6):138-41. PubMed ID: 1077005
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.