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6. Hereditary ectodermal dysplasia: report of a case. Alexander WN; Cahill RJ ASDC J Dent Child; 1969; 36(4):265 passim. PubMed ID: 4893602 [No Abstract] [Full Text] [Related]
7. Hypocalcification type amelogenesis imperfecta in permanent dentition in association with heavily worn primary teeth, gingival hyperplasia, hypodontia and impacted teeth. Atasu M; Biren S; Mumcu G J Clin Pediatr Dent; 1999; 23(2):117-21. PubMed ID: 10204452 [TBL] [Abstract][Full Text] [Related]
8. Common genetic defects of the mouth. Sanger RG Dent Assist (1931); 1975 Jun; 44(6):20-6. PubMed ID: 1074365 [No Abstract] [Full Text] [Related]
9. [Dental malformations]. Robert JM Rev Orthop Dento Faciale; 1976 Jan; 10(1):21-40. PubMed ID: 1078113 [No Abstract] [Full Text] [Related]
10. [Amelogenesis imperfecta: a case report with impactions, resorption and denticles]. Swerin I; Saietz L Tandlaegebladet; 1987 Mar; 91(5):175-8. PubMed ID: 3473723 [No Abstract] [Full Text] [Related]
11. Hypohidrotic ectodermal dysplasia with bilateral impacted teeth at the coronoid process: a case rehabilitated with mini dental implants. Güler N; Cildir S; Iseri U; Sandalli N; Dilek O Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2005 May; 99(5):E34-8. PubMed ID: 15829868 [TBL] [Abstract][Full Text] [Related]
12. Odontoonychodermal dysplasia: a previously apparently undescribed ectodermal dysplasia. Fadhil M; Ghabra TA; Deeb M; Der Kaloustian VM Am J Med Genet; 1983 Feb; 14(2):335-46. PubMed ID: 6837628 [TBL] [Abstract][Full Text] [Related]
13. Amelogenesis imperfecta and multiple impactions. Fritz GW Oral Surg Oral Med Oral Pathol; 1981 Apr; 51(4):460. PubMed ID: 6940086 [No Abstract] [Full Text] [Related]
14. A case of amelogenesis imperfecta. Edward S; Nord CE Sven Tandlak Tidskr; 1974; 67(4):229-37. PubMed ID: 4528378 [No Abstract] [Full Text] [Related]
15. Dental development in amelogenesis imperfecta: a controlled study. Seow WK Pediatr Dent; 1995; 17(1):26-30. PubMed ID: 7899098 [TBL] [Abstract][Full Text] [Related]
17. Amelogenesis imperfecta and nephrocalcinosis syndrome: a case report and review of the literature. Martelli-Júnior H; dos Santos Neto PE; de Aquino SN; de Oliveira Santos CC; Borges SP; Oliveira EA; Lopes MA; Coletta RD Nephron Physiol; 2011; 118(3):p62-5. PubMed ID: 21212699 [TBL] [Abstract][Full Text] [Related]
18. Autotransplantation of teeth in cleidocranial dysostosis. Nordenram A Odontol Revy; 1971; 22(4):363-9. PubMed ID: 5292152 [No Abstract] [Full Text] [Related]
19. New form of hidrotic ectodermal dysplasia in a Lebanese family. Mégarbané A; Noujeim Z; Fabre M; Der Kaloustian VM Am J Med Genet; 1998 Jan; 75(2):196-9. PubMed ID: 9450885 [TBL] [Abstract][Full Text] [Related]
20. Case report of a rare syndrome associating amelogenesis imperfecta and nephrocalcinosis in a consanguineous family. Paula LM; Melo NS; Silva Guerra EN; Mestrinho DH; Acevedo AC Arch Oral Biol; 2005 Feb; 50(2):237-42. PubMed ID: 15721155 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]