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 *

102 related articles for article (PubMed ID: 8723718)

  • 1. Dominantly and recessively inherited cornea plana congenita map to the same small region of chromosome 12.
    Tahvanainen E; Villanueva AS; Forsius H; Salo P; de la Chapelle A
    Genome Res; 1996 Apr; 6(4):249-54. PubMed ID: 8723718
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysis.
    Tahvanainen E; Forsius H; Karila E; Ranta S; Eerola M; Weissenbach J; Sistonen P; de la Chapelle A
    Genomics; 1995 Mar; 26(2):290-3. PubMed ID: 7601455
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The genetics of cornea plana congenita.
    Tahvanainen E; Forsius H; Kolehmainen J; Damsten M; Fellman J; de la Chapelle A
    J Med Genet; 1996 Feb; 33(2):116-9. PubMed ID: 8929947
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Linkage disequilibrium mapping of the cornea plana congenita gene CNA2.
    Tahvanainen E; Forsius H; Damsten M; Karila E; Kolehmainen J; Weissenbach J; Sistonen P; de la Chapelle A
    Genomics; 1995 Dec; 30(3):409-14. PubMed ID: 8825624
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and molecular characterization of a patient with an interstitial deletion of chromosome 12q15-q23 and peripheral corneal abnormalities.
    Tocyap ML; Azar N; Chen T; Wiggs J
    Am J Ophthalmol; 2006 Mar; 141(3):566-567. PubMed ID: 16490510
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2.
    Aldave AJ; Sonmez B; Bourla N; Schultz G; Papp JC; Salem AK; Rayner SA; Yellore VS
    Ophthalmic Genet; 2007 Jun; 28(2):57-67. PubMed ID: 17558846
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Autosomal recessive cornea plana. A clinical and genetic study of 78 cases in Finland.
    Forsius H; Damsten M; Eriksson AW; Fellman J; Lindh S; Tahvanainen E
    Acta Ophthalmol Scand; 1998 Apr; 76(2):196-203. PubMed ID: 9591953
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in KERA, encoding keratocan, cause cornea plana.
    Pellegata NS; Dieguez-Lucena JL; Joensuu T; Lau S; Montgomery KT; Krahe R; Kivelä T; Kucherlapati R; Forsius H; de la Chapelle A
    Nat Genet; 2000 May; 25(1):91-5. PubMed ID: 10802664
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Exclusion of AR-CHED from the chromosome 20 region containing the PPMD and AD-CHED loci.
    Kanis AB; Al-Rajhi AA; Taylor CM; Mathers WD; Folberg RY; Nishimura DY; Sheffield VC; Stone EM
    Ophthalmic Genet; 1999 Dec; 20(4):243-9. PubMed ID: 10617922
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mapping.
    Hand CK; Harmon DL; Kennedy SM; FitzSimon JS; Collum LM; Parfrey NA
    Genomics; 1999 Oct; 61(1):1-4. PubMed ID: 10512674
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC.
    Aldave AJ; Rosenwasser GO; Yellore VS; Papp JC; Sobel EM; Pham MN; Chen MC; Dandekar S; Sripracha R; Rayner SA; Sassani JW; Gorin MB
    Invest Ophthalmol Vis Sci; 2010 Aug; 51(8):4006-12. PubMed ID: 20357198
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical and molecular characterization of a family with autosomal recessive cornea plana.
    Ebenezer ND; Patel CB; Hariprasad SM; Chen LL; Patel RJ; Hardcastle AJ; Allen RC
    Arch Ophthalmol; 2005 Sep; 123(9):1248-53. PubMed ID: 16157807
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Recessive cornea plana in the Kingdom of Saudi Arabia.
    Khan AO; Aldahmesh M; Meyer B
    Ophthalmology; 2006 Oct; 113(10):1773-8. PubMed ID: 17011957
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Three autosomal dominant corneal dystrophies map to chromosome 5q.
    Stone EM; Mathers WD; Rosenwasser GO; Holland EJ; Folberg R; Krachmer JH; Nichols BE; Gorevic PD; Taylor CM; Streb LM
    Nat Genet; 1994 Jan; 6(1):47-51. PubMed ID: 8136834
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A COL17A1 Splice-Altering Mutation Is Prevalent in Inherited Recurrent Corneal Erosions.
    Oliver VF; van Bysterveldt KA; Cadzow M; Steger B; Romano V; Markie D; Hewitt AW; Mackey DA; Willoughby CE; Sherwin T; Crosier PS; McGhee CN; Vincent AL
    Ophthalmology; 2016 Apr; 123(4):709-22. PubMed ID: 26786512
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Linkage mapping of Thiel-Behnke corneal dystrophy (CDB2) to chromosome 10q23-q24.
    Yee RW; Sullivan LS; Lai HT; Stock EL; Lu Y; Khan MN; Blanton SH; Daiger SP
    Genomics; 1997 Nov; 46(1):152-4. PubMed ID: 9403072
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Allelic and locus heterogeneity in autosomal recessive gelatinous drop-like corneal dystrophy.
    Ren Z; Lin PY; Klintworth GK; Iwata F; Munier FL; Schorderet DF; El Matri L; Theendakara V; Basti S; Reddy M; Hejtmancik JF
    Hum Genet; 2002 Jun; 110(6):568-77. PubMed ID: 12107443
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Delineation of a 1-cM region on distal 5q containing the locus for corneal dystrophies Groenouw type I and lattice type I and exclusion of the candidate genes SPARC and LOX.
    Korvatska E; Munier FL; Zografos L; Ahmad F; Faggioni R; Dolivo-Beuret A; Uffer S; Pescia G; Schorderet DF
    Eur J Hum Genet; 1996; 4(4):214-8. PubMed ID: 8875187
    [TBL] [Abstract][Full Text] [Related]  

  • 19. High prevalence of posterior polymorphous corneal dystrophy in the Czech Republic; linkage disequilibrium mapping and dating an ancestral mutation.
    Liskova P; Gwilliam R; Filipec M; Jirsova K; Reinstein Merjava S; Deloukas P; Webb TR; Bhattacharya SS; Ebenezer ND; Morris AG; Hardcastle AJ
    PLoS One; 2012; 7(9):e45495. PubMed ID: 23049806
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Linkage of congenital hereditary endothelial dystrophy to chromosome 20.
    Toma NM; Ebenezer ND; Inglehearn CF; Plant C; Ficker LA; Bhattacharya SS
    Hum Mol Genet; 1995 Dec; 4(12):2395-8. PubMed ID: 8634716
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.