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.
113 related articles for article (PubMed ID: 1069908)
1. [A familial strain of amelogenesis imperfecta hypoplastic type with dominant x-linked heredity]. Cassese M; Grulliero A; Di Napoli G; Ventruto V Minerva Stomatol; 1976; 25(2):89-94. PubMed ID: 1069908 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. Demonstration of the lyon hypothesis in X-linked dominant hypoplastic amelogenesis imperfecta. Berkman MD; Singer A Birth Defects Orig Artic Ser; 1971 Jun; 7(7):204-9. PubMed ID: 5173207 [TBL] [Abstract][Full Text] [Related]
4. [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]
5. 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]
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]
8. 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]
9. 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]
10. [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]
13. Enamelin (Enam) is essential for amelogenesis: ENU-induced mouse mutants as models for different clinical subtypes of human amelogenesis imperfecta (AI). Masuya H; Shimizu K; Sezutsu H; Sakuraba Y; Nagano J; Shimizu A; Fujimoto N; Kawai A; Miura I; Kaneda H; Kobayashi K; Ishijima J; Maeda T; Gondo Y; Noda T; Wakana S; Shiroishi T Hum Mol Genet; 2005 Mar; 14(5):575-83. PubMed ID: 15649948 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Mapping of the locus for autosomal dominant amelogenesis imperfecta (AIH2) to a 4-Mb YAC contig on chromosome 4q11-q21. Kärrman C; Bäckman B; Dixon M; Holmgren G; Forsman K Genomics; 1997 Jan; 39(2):164-70. PubMed ID: 9027503 [TBL] [Abstract][Full Text] [Related]
16. Amelogenesis imperfecta among Israeli Jews and the description of a new type of local hypoplastic autosomal recessive amelogenesis imperfecta. Chosack A; Eidelman E; Wisotski I; Cohen T Oral Surg Oral Med Oral Pathol; 1979 Feb; 47(2):148-56. PubMed ID: 284277 [TBL] [Abstract][Full Text] [Related]