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9. Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutation. Ravassipour DB; Hart PS; Hart TC; Ritter AV; Yamauchi M; Gibson C; Wright JT J Dent Res; 2000 Jul; 79(7):1476-81. PubMed ID: 11005731 [TBL] [Abstract][Full Text] [Related]
10. X-linked amelogenesis imperfecta may result from decreased formation of tyrosine rich amelogenin peptide (TRAP). Li W; Gao C; Yan Y; DenBesten P Arch Oral Biol; 2003 Mar; 48(3):177-83. PubMed ID: 12648554 [TBL] [Abstract][Full Text] [Related]
11. Transgenic mice that express normal and mutated amelogenins. Gibson CW; Yuan ZA; Li Y; Daly B; Suggs C; Aragon MA; Alawi F; Kulkarni AB; Wright JT J Dent Res; 2007 Apr; 86(4):331-5. PubMed ID: 17384027 [TBL] [Abstract][Full Text] [Related]
12. Detection of a novel mutation in X-linked amelogenesis imperfecta. Kindelan SA; Brook AH; Gangemi L; Lench N; Wong FS; Fearne J; Jackson Z; Foster G; Stringer BM J Dent Res; 2000 Dec; 79(12):1978-82. PubMed ID: 11201048 [TBL] [Abstract][Full Text] [Related]
13. Enamel ultrastructure and protein content in X-linked amelogenesis imperfecta. Wright JT; Aldred MJ; Crawford PJ; Kirkham J; Robinson C Oral Surg Oral Med Oral Pathol; 1993 Aug; 76(2):192-9. PubMed ID: 8361731 [TBL] [Abstract][Full Text] [Related]
14. Amelogenin signal peptide mutation: correlation between mutations in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfecta. Lagerström-Fermér M; Nilsson M; Bäckman B; Salido E; Shapiro L; Pettersson U; Landegren U Genomics; 1995 Mar; 26(1):159-62. PubMed ID: 7782077 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Relationship of phenotype and genotype in X-linked amelogenesis imperfecta. Wright JT; Hart PS; Aldred MJ; Seow K; Crawford PJ; Hong SP; Gibson CW; Hart TC Connect Tissue Res; 2003; 44 Suppl 1():72-8. PubMed ID: 12952177 [TBL] [Abstract][Full Text] [Related]
18. Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6. Hu JC; Chan HC; Simmer SG; Seymen F; Richardson AS; Hu Y; Milkovich RN; Estrella NM; Yildirim M; Bayram M; Chen CF; Simmer JP PLoS One; 2012; 7(12):e52052. PubMed ID: 23251683 [TBL] [Abstract][Full Text] [Related]
20. [Alteración del gen AMELX en amelogénesis imperfecta. Una breve revisión]. Tremillo-Maldonado O; Molina-Frechero N; González-González R; Bologna-Molina R Gac Med Mex; 2019; 155(1):101-107. PubMed ID: 30799455 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]