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)

  • 1. [Hereditary disorders of enamel development].
    Beliakov IuA; Blokhina MI; Krotov VA
    Stomatologiia (Mosk); 1986; 65(3):88-9. PubMed ID: 3523848
    [No Abstract]   [Full Text] [Related]  

  • 2. Enamel hypoplasia and anomalies of the enamel.
    Winter GB; Brook AH
    Dent Clin North Am; 1975 Jan; 19(1):3-24. PubMed ID: 162891
    [No Abstract]   [Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A particular type of dominant hereditary enamel dysplasia?].
    Weyers H
    Dtsch Zahnarztl Z; 1977 Mar; 32(3):243-7. PubMed ID: 265269
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Genetic studies on X-chromosomal, incompletely dominant hypoplasia of tooth enamel].
    Kalden M
    Dtsch Zahnarztl Z; 1988 Nov; 43(11):1177-81. PubMed ID: 3251735
    [No Abstract]   [Full Text] [Related]  

  • 6. Hereditary amelogenesis imperfecta. An epidemiological, genetic and clinical study in a Swedish child population.
    Sundell S
    Swed Dent J Suppl; 1986; 31():1-38. PubMed ID: 3460191
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The effects of acid-etching on enamel from different clinical variants of amelogenesis imperfecta: an SEM study.
    Seow WK; Amaratunge A
    Pediatr Dent; 1998; 20(1):37-42. PubMed ID: 9524971
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Hereditary type enamel hypoplasia. Clinical and histopathological findings of an observed case].
    Debernardi C; Pirrello D
    Minerva Stomatol; 1989 Mar; 38(3):321-34. PubMed ID: 2657367
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Regularly dominant autosomal enamel hypoplasia with a frontal open bite: chance or pleiotropy?].
    Tammoscheit UG
    ZWR; 1979 Nov; 88(21):952, 955-6. PubMed ID: 294008
    [No Abstract]   [Full Text] [Related]  

  • 10. Hereditary enamel hypoplasia.
    Torres-Laz MS
    J Philipp Dent Assoc; 1998; 50(2):18-21. PubMed ID: 10597144
    [No Abstract]   [Full Text] [Related]  

  • 11. [A case report of hereditary amelogenesis imperfecta in a family (author's transl)].
    Minegishi H; Irie E; Osaka N; Moriyama K; Sano M; Ito H; Hamamoto Y; Goto H
    Josai Shika Daigaku Kiyo; 1979; 8(3):413-7. PubMed ID: 297513
    [No Abstract]   [Full Text] [Related]  

  • 12. Enamel dysplasia and caries.
    Roelike H
    IDAA Commun; 1975 Oct; 10(1):2-4, 21. PubMed ID: 1072410
    [No Abstract]   [Full Text] [Related]  

  • 13. [Changes in the enamel structure of permanent teeth acquired during amelogenesis].
    Montagne F
    Inf Dent; 1985 Apr; 67(15):1417-29. PubMed ID: 3863790
    [No Abstract]   [Full Text] [Related]  

  • 14. Ataxia, mental deterioration, epilepsy in a family with dominant enamel hypoplasia: a variant of Kohlschütter-Tönz syndrome?
    Guazzi G; Palmeri S; Malandrini A; Ciacci G; Di Perri R; Mancini G; Messina C; Salvadori C
    Am J Med Genet; 1994 Mar; 50(1):79-83. PubMed ID: 8160757
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Inherited defects in tooth structure.
    Witkop CJ; Rao S
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):153-84. PubMed ID: 4375507
    [No Abstract]   [Full Text] [Related]  

  • 16. [An enamel disorder in two siblings].
    Créton MA; Cune MS
    Ned Tijdschr Tandheelkd; 2004 Oct; 111(10):400-2. PubMed ID: 15553370
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Four cases of inherited enamel hypoplasia.
    Neiburger EJ
    Gen Dent; 1990; 38(1):46-8. PubMed ID: 2376319
    [No Abstract]   [Full Text] [Related]  

  • 18. The structure and composition of deciduous enamel affected by local hypoplastic autosomal dominant amelogenesis imperfecta resulting from an ENAM mutation.
    Shore RC; Bäckman B; Elcock C; Brook AH; Brookes SJ; Kirkham J
    Cells Tissues Organs; 2010; 191(4):301-6. PubMed ID: 19923784
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The molecular basis of hereditary enamel defects in humans.
    Wright JT; Carrion IA; Morris C
    J Dent Res; 2015 Jan; 94(1):52-61. PubMed ID: 25389004
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hypoplastic-hypomaturation amelogenesis imperfecta with taurodontism: report of case.
    Parker JL; Regattieri LR; Thomas JP
    ASDC J Dent Child; 1975; 42(5):379-83. PubMed ID: 1100695
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.