BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

234 related articles for article (PubMed ID: 8529675)

  • 1. Aniridia: recent achievements in paediatric practice.
    Ivanov I; Shuper A; Shohat M; Snir M; Weitz R
    Eur J Pediatr; 1995 Oct; 154(10):795-800. PubMed ID: 8529675
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Molecular genetic study of the PAX6 gene in aniridia patients].
    Wolf M; Zabel B; Lorenz B; Blankenagel A; Ghorbani MB; Schwenn O; Wildhardt G
    Ophthalmologe; 1998 Dec; 95(12):828-30. PubMed ID: 10025146
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Two neonates with congenital aniridia: the necessity of genetic investigation].
    van Os E; Niemarkt HJ; Verreussel MJ; Cruysberg JR; Bok LA; Spruijt L
    Ned Tijdschr Geneeskd; 2008 Mar; 152(10):569-73. PubMed ID: 18402324
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia.
    Dubey SK; Mahalaxmi N; Vijayalakshmi P; Sundaresan P
    Mol Vis; 2015; 21():88-97. PubMed ID: 25678763
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Aniridia: current pathology and management.
    Lee H; Khan R; O'Keefe M
    Acta Ophthalmol; 2008 Nov; 86(7):708-15. PubMed ID: 18937825
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ten novel mutations found in Aniridia.
    Wolf MT; Lorenz B; Winterpacht A; Drechsler M; Schumacher V; Royer-Pokora B; Blankenagel A; Zabel B; Wildhardt G
    Hum Mutat; 1998; 12(5):304-13. PubMed ID: 9792406
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutation in the PAX6 gene in twenty patients with aniridia.
    Chao LY; Huff V; Strong LC; Saunders GF
    Hum Mutat; 2000; 15(4):332-9. PubMed ID: 10737978
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene.
    Glaser T; Walton DS; Maas RL
    Nat Genet; 1992 Nov; 2(3):232-9. PubMed ID: 1345175
    [TBL] [Abstract][Full Text] [Related]  

  • 9. PAX6 3' deletion in a family with aniridia.
    Wawrocka A; Budny B; Debicki S; Jamsheer A; Sowinska A; Krawczynski MR
    Ophthalmic Genet; 2012 Mar; 33(1):44-8. PubMed ID: 21985185
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic analysis of chromosome 11p13 and the PAX6 gene in a series of 125 cases referred with aniridia.
    Robinson DO; Howarth RJ; Williamson KA; van Heyningen V; Beal SJ; Crolla JA
    Am J Med Genet A; 2008 Mar; 146A(5):558-69. PubMed ID: 18241071
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Polymerase chain reaction-based risk assessment for Wilms tumor in sporadic aniridia.
    Gupta SK; De Becker I; Guernsey DL; Neumann PE
    Am J Ophthalmol; 1998 May; 125(5):687-92. PubMed ID: 9625553
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Paired box mutations in familial and sporadic aniridia predicts truncated aniridia proteins.
    Martha A; Ferrell RE; Mintz-Hittner H; Lyons LA; Saunders GF
    Am J Hum Genet; 1994 May; 54(5):801-11. PubMed ID: 7909985
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Three novel aniridia mutations in the human PAX6 gene.
    Martha A; Strong LC; Ferrell RE; Saunders GF
    Hum Mutat; 1995; 6(1):44-9. PubMed ID: 7550230
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Frequent chromosome aberrations revealed by molecular cytogenetic studies in patients with aniridia.
    Crolla JA; van Heyningen V
    Am J Hum Genet; 2002 Nov; 71(5):1138-49. PubMed ID: 12386836
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ocular findings in Gillespie-like syndrome: association with a new PAX6 mutation.
    Ticho BH; Hilchie-Schmidt C; Egel RT; Traboulsi EI; Howarth RJ; Robinson D
    Ophthalmic Genet; 2006 Dec; 27(4):145-9. PubMed ID: 17148041
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 11p13 deletions can be more frequent than the PAX6 gene point mutations in Polish patients with aniridia.
    Wawrocka A; Sikora A; Kuszel L; Krawczynski MR
    J Appl Genet; 2013 Aug; 54(3):345-51. PubMed ID: 23761016
    [TBL] [Abstract][Full Text] [Related]  

  • 17. PAX6 mutation in association with ptosis, cataract, iris hypoplasia, corneal opacification and diabetes: a new variant of familial aniridia?
    Peter NM; Leyland M; Mudhar HS; Lowndes J; Owen KR; Stewart H
    Clin Exp Ophthalmol; 2013 Dec; 41(9):835-41. PubMed ID: 23566044
    [TBL] [Abstract][Full Text] [Related]  

  • 18. PAX6 aniridia and interhemispheric brain anomalies.
    Abouzeid H; Youssef MA; ElShakankiri N; Hauser P; Munier FL; Schorderet DF
    Mol Vis; 2009 Oct; 15():2074-83. PubMed ID: 19862335
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Absence of PAX6 gene mutations in Gillespie syndrome (partial aniridia, cerebellar ataxia, and mental retardation).
    Glaser T; Ton CC; Mueller R; Petzl-Erler ML; Oliver C; Nevin NC; Housman DE; Maas RL
    Genomics; 1994 Jan; 19(1):145-8. PubMed ID: 8188215
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.