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 *

120 related articles for article (PubMed ID: 6978612)

  • 21. [Current status of linkage studies for gene localization in corneal dystrophies].
    Lisch W; Weidle EG; Emmig CT; Kömpf J; Baur MP
    Fortschr Ophthalmol; 1991; 88(2):105-6. PubMed ID: 1855722
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Endothelial dystrophy, iris hypoplasia, congenital cataract, and stromal thinning (edict) syndrome maps to chromosome 15q22.1-q25.3.
    Jun AS; Broman KW; Do DV; Akpek EK; Stark WJ; Gottsch JD
    Am J Ophthalmol; 2002 Aug; 134(2):172-6. PubMed ID: 12140022
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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]  

  • 25. Linkage of a gene for macular corneal dystrophy to chromosome 16.
    Vance JM; Jonasson F; Lennon F; Sarrica J; Damji KF; Stauffer J; Pericak-Vance MA; Klintworth GK
    Am J Hum Genet; 1996 Apr; 58(4):757-62. PubMed ID: 8644739
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Pseudokeratoconus in trisomy 21 and posterior polymorphous corneal dystrophy].
    Lang GK; Holbach L; Schlötzer U
    Klin Monbl Augenheilkd; 1989 Aug; 195(2):95-9. PubMed ID: 2529395
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genetic linkage of Francois-Neetens fleck (mouchetée) corneal dystrophy to chromosome 2q35.
    Jiao X; Munier FL; Schorderet DF; Zografos L; Smith J; Rubin B; Hejtmancik JF
    Hum Genet; 2003 May; 112(5-6):593-9. PubMed ID: 12607114
    [TBL] [Abstract][Full Text] [Related]  

  • 28. North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the
    Bowne SJ; Sullivan LS; Wheaton DK; Locke KG; Jones KD; Koboldt DC; Fulton RS; Wilson RK; Blanton SH; Birch DG; Daiger SP
    Mol Vis; 2016; 22():1239-1247. PubMed ID: 27777503
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The MNSs blood groups of families with chromosome 4 rearrangements.
    Cook PJ; Lindenbaum RH; Salonen R; de la Chapelle A; Daker MG; Buckton KE; Noades JE; Tippett P
    Ann Hum Genet; 1981 Feb; 45(1):39-47. PubMed ID: 7316476
    [No Abstract]   [Full Text] [Related]  

  • 30. Linkage analysis in dominant optic atrophy.
    Kivlin JD; Lovrien EW; Bishop DT; Maumenee IH
    Am J Hum Genet; 1983 Nov; 35(6):1190-5. PubMed ID: 6580816
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. 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]  

  • 33. Mutation hot spots in 5q31-linked corneal dystrophies.
    Korvatska E; Munier FL; Djemaï A; Wang MX; Frueh B; Chiou AG; Uffer S; Ballestrazzi E; Braunstein RE; Forster RK; Culbertson WW; Boman H; Zografos L; Schorderet DF
    Am J Hum Genet; 1998 Feb; 62(2):320-4. PubMed ID: 9463327
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Heredofamilial corneal dystrophies].
    François J
    Ber Zusammenkunft Dtsch Ophthalmol Ges; 1972; 71():171-222. PubMed ID: 4126168
    [No Abstract]   [Full Text] [Related]  

  • 35. 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]  

  • 36. Linkage analysis in lattice corneal dystrophy.
    Kivlin JD; Lovrien EW; Maumenee IH; Bishop DT; Bias W
    Am J Med Genet; 1984 Oct; 19(2):387-90. PubMed ID: 6334443
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A new corneal disease with recurrent erosive episodes and autosomal-dominant inheritance.
    Hammar B; Björck E; Lagerstedt K; Dellby A; Fagerholm P
    Acta Ophthalmol; 2008 Nov; 86(7):758-63. PubMed ID: 18778339
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Autosomal dominant ophthalmologic disorders and linkage.
    Hittner HM; Ferrell RE
    J Pediatr Ophthalmol Strabismus; 1982; 19(1):40-7. PubMed ID: 6802952
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Linkage relations of the locus for granular corneal dystrophy Groenouw type I with 35 polymorphic systems.
    Møller HU; Eiberg H; Kruse TA
    Acta Ophthalmol (Copenh); 1989 Dec; 67(6):721-3. PubMed ID: 2618643
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 6.