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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

227 related articles for article (PubMed ID: 10669095)

  • 1. Mutational analysis of X-linked amelogenesis imperfecta in multiple families.
    Hart S; Hart T; Gibson C; Wright JT
    Arch Oral Biol; 2000 Jan; 45(1):79-86. PubMed ID: 10669095
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutations.
    Hart PS; Aldred MJ; Crawford PJ; Wright NJ; Hart TC; Wright JT
    Arch Oral Biol; 2002 Apr; 47(4):261-5. PubMed ID: 11922869
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A new frameshift mutation encoding a truncated amelogenin leads to X-linked amelogenesis imperfecta.
    Greene SR; Yuan ZA; Wright JT; Amjad H; Abrams WR; Buchanan JA; Trachtenberg DI; Gibson CW
    Arch Oral Biol; 2002 Mar; 47(3):211-7. PubMed ID: 11839357
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular biology of hereditary enamel defects.
    Aldred MJ; Crawford PJ
    Ciba Found Symp; 1997; 205():200-5; discussion 205-9. PubMed ID: 9189626
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An amelogenin gene defect associated with human X-linked amelogenesis imperfecta.
    Collier PM; Sauk JJ; Rosenbloom SJ; Yuan ZA; Gibson CW
    Arch Oral Biol; 1997 Mar; 42(3):235-42. PubMed ID: 9188994
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1).
    Lench NJ; Winter GB
    Hum Mutat; 1995; 5(3):251-9. PubMed ID: 7599636
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1).
    Aldred MJ; Crawford PJ; Roberts E; Thomas NS
    Hum Genet; 1992 Dec; 90(4):413-6. PubMed ID: 1483698
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical features of a family with X-linked amelogenesis imperfecta mapping to a new locus (AIH3) on the long arm of the X chromosome.
    Crawford PJ; Aldred MJ
    Oral Surg Oral Med Oral Pathol; 1993 Aug; 76(2):187-91. PubMed ID: 8361730
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. DNA diagnosis of X-linked amelogenesis imperfecta (AIH1).
    Lench NJ; Brook AH
    J Oral Pathol Med; 1997 Mar; 26(3):135-7. PubMed ID: 9083938
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. A nomenclature for X-linked amelogenesis imperfecta.
    Hart PS; Hart TC; Simmer JP; Wright JT
    Arch Oral Biol; 2002 Apr; 47(4):255-60. PubMed ID: 11922868
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutation.
    Haubek D; Gjørup H; Jensen LG; Juncker I; Nyegaard M; Børglum AD; Poulsen S; Hertz JM
    Int J Paediatr Dent; 2011 Nov; 21(6):407-12. PubMed ID: 21702852
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Inherited enamel defects.
    Bäckman B
    Ciba Found Symp; 1997; 205():175-82; discussion 183-6. PubMed ID: 9189624
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1).
    Lagerström M; Dahl N; Nakahori Y; Nakagome Y; Bäckman B; Landegren U; Pettersson U
    Genomics; 1991 Aug; 10(4):971-5. PubMed ID: 1916828
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular analysis for genetic counselling in amelogenesis imperfecta.
    Aldred MJ; Hall RK; Kilpatrick N; Bankier A; Savarirayan R; Lamandé SR; Lench NJ; Crawford PJ
    Oral Dis; 2002 Sep; 8(5):249-53. PubMed ID: 12363109
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta.
    Kim JW; Simmer JP; Hu YY; Lin BP; Boyd C; Wright JT; Yamada CJ; Rayes SK; Feigal RJ; Hu JC
    J Dent Res; 2004 May; 83(5):378-83. PubMed ID: 15111628
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.