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42. Scanning electron microscopic study of hypoplastic type amelogenesis imperfecta in primary teeth. Uzamis M; Celik H; Erkmen N; Batirbaygil Y J Clin Pediatr Dent; 1997; 21(3):265-8. PubMed ID: 9484138 [TBL] [Abstract][Full Text] [Related]
43. A family with oculodentodigital dysplasia. Weintraub DM; Baum JL; Pashayan HM Cleft Palate J; 1975 Jul; 12():323-9. PubMed ID: 1057461 [TBL] [Abstract][Full Text] [Related]
44. [Inheritance identification by studying geneology of amelogenesis imperfecta]. Kostić A Stomatol Vjesn; 1968; 2(1-6):165-7. PubMed ID: 5293736 [No Abstract] [Full Text] [Related]
46. [A family with hereditary hypofibrinogenemia]. Pfluger N; Gehrig D Schweiz Med Wochenschr; 1977 Oct; 107(41):1454-5. PubMed ID: 918595 [TBL] [Abstract][Full Text] [Related]
47. [Amelogenesis imperfecta recorded in four generations of one family]. Dordević S; Kostić M; Mitrović T; Trisović D; Ivancević J Stomatol Glas Srb; 1981; 28(2):111-4. PubMed ID: 6947578 [No Abstract] [Full Text] [Related]
48. Dental management of amelogenesis imperfecta patients: a primer on genotype-phenotype correlations. Ng FK; Messer LB Pediatr Dent; 2009; 31(1):20-30. PubMed ID: 19320256 [TBL] [Abstract][Full Text] [Related]
49. Clinical and radiographic features of a family with autosomal dominant amelogenesis imperfecta with taurodontism. Aldred MJ; Savarirayan R; Lamandé SR; Crawford PJ Oral Dis; 2002 Jan; 8(1):62-8. PubMed ID: 11936459 [TBL] [Abstract][Full Text] [Related]
50. Restoring function and esthetics in a patient with amelogenesis imperfecta: a case report. Sengun A; Ozer F Quintessence Int; 2002 Mar; 33(3):199-204. PubMed ID: 11921768 [TBL] [Abstract][Full Text] [Related]
51. [Recurrent familial neuropathy: report of one family]. Hinault P; Menault F; Le Marec B; Sabouraud O J Genet Hum; 1981 Dec; 29(4):409-17. PubMed ID: 7328415 [TBL] [Abstract][Full Text] [Related]
52. Namaqualand hip dysplasia: an autosomal dominant entity. Beighton P; Christy G; Learmonth ID Am J Med Genet; 1984 Sep; 19(1):161-9. PubMed ID: 6496567 [TBL] [Abstract][Full Text] [Related]
53. Amelogenesis imperfecta: a case report. Ogunyinka A West Afr J Med; 2001; 20(1):61-4. PubMed ID: 11505891 [TBL] [Abstract][Full Text] [Related]
54. PCR detection of the human amelogenin gene and its application to the diagnosis of amelogenesis imperfecta. Sekiguchi H; Minaguchi K; Machida Y; Yakushiji M Bull Tokyo Dent Coll; 1998 Nov; 39(4):275-85. PubMed ID: 10218009 [TBL] [Abstract][Full Text] [Related]
56. [Some considerations on 2 cases of amelogenesis imperfecta]. Jannarone F Rass Int Stomatol Prat; 1967; 18(1):51-9. PubMed ID: 5228174 [No Abstract] [Full Text] [Related]
57. Hereditary aspects and classification of hereditary amelogenesis imperfecta. Sundell S; Valentin J Community Dent Oral Epidemiol; 1986 Aug; 14(4):211-6. PubMed ID: 3461907 [TBL] [Abstract][Full Text] [Related]
58. Investigation of the aetiopathogenesis of amelogenesis imperfecta through microscopic, submicroscopic and cytogenetic methods--a case report. Koray F; Soyman M; Erdoğan G J Oral Rehabil; 1988 Mar; 15(2):149-62. PubMed ID: 2836577 [TBL] [Abstract][Full Text] [Related]
59. [Observations of familial cases of amelogenesis imperfecta and a critical review]. Bertelli E; Ferrari M; Corsi S; Berti M Minerva Stomatol; 1987 Nov; 36(11):823-8. PubMed ID: 3323869 [No Abstract] [Full Text] [Related]
60. A syndrome of epilepsy, dementia, and amelogenesis imperfecta: genetic and clinical features. Christodoulou J; Hall RK; Menahem S; Hopkins IJ; Rogers JG J Med Genet; 1988 Dec; 25(12):827-30. PubMed ID: 3236364 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]