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 *

85 related articles for article (PubMed ID: 4510007)

  • 1. 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]  

  • 2. Hereditary hypocalcified amelogenesis imperfecta. Pedigree analysis.
    Chabora AJ; Berkman MD; Horowitz SL; Nahoum HI
    Oral Surg Oral Med Oral Pathol; 1972 Jun; 33(6):922-5. PubMed ID: 4503458
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. A multidisciplinary approach for the diagnosis of hypocalcified amelogenesis imperfecta in two Chilean families.
    Urzúa B; Ortega-Pinto A; Farias DA; Franco E; Morales-Bozo I; Moncada G; Escobar-Pezoa N; Scholz U; Cifuentes V
    Acta Odontol Scand; 2012 Jan; 70(1):7-14. PubMed ID: 21504268
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutation.
    Haubek D; Gjørup H; Jensen LG; Juncker I; Nyegaard M; Børglum AD; Poulsen S; Hertz JM
    Int J Paediatr Dent; 2011 Nov; 21(6):407-12. PubMed ID: 21702852
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 21(4):341-55. PubMed ID: 9484124
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hypoplastic amelogenesis imperfecta: report of case.
    Fischman SL; Fischman BC
    J Am Dent Assoc; 1967 Oct; 75(4):929-31. PubMed ID: 5233412
    [No Abstract]   [Full Text] [Related]  

  • 8. Hereditary amelogenesis imperfecta.
    Laird WR
    Dent Pract Dent Rec; 1968 Nov; 19(3):90-2. PubMed ID: 5247082
    [No Abstract]   [Full Text] [Related]  

  • 9. Amelogenesis imperfecta. Report of two cases.
    Druck JS
    Oral Surg Oral Med Oral Pathol; 1975 Mar; 39(3):502-5. PubMed ID: 1054149
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hypocalcified type of amelogenesis imperfecta in a large family: clinical, radiographic, and histological findings, associated dento-facial anomalies, and resulting treatment load.
    Gjørup H; Haubek D; Hintze H; Haukali G; Løvschall H; Hertz JM; Poulsen S
    Acta Odontol Scand; 2009; 67(4):240-7. PubMed ID: 19452331
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Overdenture as a restorative option for hypocalcified-hypoplastic amelogenesis imperfecta: a case report.
    Assunção WG; Barão VA; Kanno CM; Saito CT; Delben JA
    J Contemp Dent Pract; 2009 May; 10(3):67-73. PubMed ID: 19430628
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta.
    Hart PS; Becerik S; Cogulu D; Emingil G; Ozdemir-Ozenen D; Han ST; Sulima PP; Firatli E; Hart TC
    Clin Genet; 2009 Apr; 75(4):401-4. PubMed ID: 19220331
    [No Abstract]   [Full Text] [Related]  

  • 13. [Amelogenesis imperfecta. Description of a clinical case].
    Villalobos S; Rivera H; Acevedo AM; Pinto-Cisternas J
    Rev ADM; 1991; 48(2):95-100. PubMed ID: 1859812
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The mineral composition and enamel ultrastructure of hypocalcified amelogenesis imperfecta.
    Wright JT; Duggal MS; Robinson C; Kirkham J; Shore R
    J Craniofac Genet Dev Biol; 1993; 13(2):117-26. PubMed ID: 8325967
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Amelogenesis imperfecta].
    Neceva Lj; Mirceva M
    God Zb Med Fak Skopje; 1974; 20():473-9. PubMed ID: 4465250
    [No Abstract]   [Full Text] [Related]  

  • 16. [Transmissible amelogenesis imperfecta. Clinical study on several subjects of the same family].
    Edé D; David P; Fortier JP
    Actual Odontostomatol (Paris); 1975 Jun; (110):297-312. PubMed ID: 1190011
    [No Abstract]   [Full Text] [Related]  

  • 17. Amelogenesis imperfecta: a case report.
    Ogunyinka A
    West Afr J Med; 2001; 20(1):61-4. PubMed ID: 11505891
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Local, hypoplastic type of amelogenesis imperfecta: a clinical, genetic, radiological and dermatoglyphic study.
    Atasu M; Genc A; Namdar F
    J Clin Pediatr Dent; 1996; 20(4):337-42. PubMed ID: 9151630
    [TBL] [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; 25(11):738-40. PubMed ID: 3236352
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel FAM20A mutation causes autosomal recessive amelogenesis imperfecta.
    Volodarsky M; Zilberman U; Birk OS
    Arch Oral Biol; 2015 Jun; 60(6):919-22. PubMed ID: 25827751
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.