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.
3. 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]
4. [Autosomal-dominant hypoplastic form of amelogenesis imperfecta]. Asikov P; Penev N; Stojanov I Stomatologiia (Sofiia); 1987; 69(5):40-3. PubMed ID: 3507107 [No Abstract] [Full Text] [Related]
5. Hypomaturation amelogenesis imperfecta: account of a family with an X-linked inheritance pattern. Bundzman ER; Modesto A Braz Dent J; 1999; 10(2):111-6. PubMed ID: 10863398 [TBL] [Abstract][Full Text] [Related]
6. Kohlschütter-Tönz syndrome: epilepsy, dementia, and amelogenesis imperfecta. Zlotogora J; Fuks A; Borochowitz Z; Tal Y Am J Med Genet; 1993 Jun; 46(4):453-4. PubMed ID: 8357021 [TBL] [Abstract][Full Text] [Related]
7. A novel autosomal-recessive mutation, whitish chalk-like teeth, resembling amelogenesis imperfecta, maps to rat chromosome 14 corresponding to human 4q21. Masuyama T; Miyajima K; Ohshima H; Osawa M; Yokoi N; Oikawa T; Taniguchi K Eur J Oral Sci; 2005 Dec; 113(6):451-6. PubMed ID: 16324133 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. [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]
10. [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]
11. Amelogenesis imperfecta: a classification and catalogue for the 21st century. Aldred MJ; Savarirayan R; Crawford PJ Oral Dis; 2003 Jan; 9(1):19-23. PubMed ID: 12617253 [TBL] [Abstract][Full Text] [Related]
12. X-linked hypomaturation type of amelogenesis imperfecta exhibiting lyonization in affected females. McLarty EL; Giansanti JS; Hibbard ED Oral Surg Oral Med Oral Pathol; 1973 Nov; 36(5):678-85. PubMed ID: 4518031 [No Abstract] [Full Text] [Related]
13. 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]
14. 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]
15. Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate. Downey LM; Keen TJ; Jalili IK; McHale J; Aldred MJ; Robertson SP; Mighell A; Fayle S; Wissinger B; Inglehearn CF Eur J Hum Genet; 2002 Dec; 10(12):865-9. PubMed ID: 12461695 [TBL] [Abstract][Full Text] [Related]
17. Exclusion of p63 as a candidate gene for autosomal-dominant amelogenesis imperfecta. Gu X; Bäckman B; Coates PJ; Cullman I; Hellman U; Lind L; Nylander K Acta Odontol Scand; 2006 Apr; 64(2):111-4. PubMed ID: 16546853 [TBL] [Abstract][Full Text] [Related]
18. Identification of a novel mutation in the enamalin gene in a family with autosomal-dominant amelogenesis imperfecta. Gutierrez SJ; Chaves M; Torres DM; Briceño I Arch Oral Biol; 2007 May; 52(5):503-6. PubMed ID: 17316551 [TBL] [Abstract][Full Text] [Related]