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 *

124 related articles for article (PubMed ID: 8275096)

  • 21. Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9.
    Ikeuchi T; Asaka T; Saito M; Tanaka H; Higuchi S; Tanaka K; Saida K; Uyama E; Mizusawa H; Fukuhara N; Nonaka I; Takamori M; Tsuji S
    Ann Neurol; 1997 Apr; 41(4):432-7. PubMed ID: 9124799
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes.
    McKay JD; Patterson B; Craig JE; Russell-Eggitt IM; Wirth MG; Burdon KP; Hewitt AW; Cohn AC; Kerdraon Y; Mackey DA
    Br J Ophthalmol; 2005 Jul; 89(7):831-4. PubMed ID: 15965161
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Linkage mapping of new X-linked juvenile retinoschisis kindreds using microsatellite markers.
    Shastry BS; Hejtmancik FJ; Margherio RT; Trese MT
    Biochem Biophys Res Commun; 1996 Mar; 220(3):824-7. PubMed ID: 8607849
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.
    Bruford EA; Riise R; Teague PW; Porter K; Thomson KL; Moore AT; Jay M; Warburg M; Schinzel A; Tommerup N; Tornqvist K; Rosenberg T; Patton M; Mansfield DC; Wright AF
    Genomics; 1997 Apr; 41(1):93-9. PubMed ID: 9126487
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Genetic analysis of familial prostatic cancer: localization of a gene predisposing to prostatic cancer (PCaP) on chromosome 1q 42.2-43].
    Valeri A; Drelon E; Paiss T; Vogel W; de Petriconi R; Hautmann R; Fournier G; Mangin P; Berthon P; Cussenot O
    Prog Urol; 1999 Sep; 9(4):680-8. PubMed ID: 10555221
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11.
    Wissinger B; Jägle H; Kohl S; Broghammer M; Baumann B; Hanna DB; Hedels C; Apfelstedt-Sylla E; Randazzo G; Jacobson SG; Zrenner E; Sharpe LT
    Genomics; 1998 Aug; 51(3):325-31. PubMed ID: 9721202
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3.
    Finckh U; Xu S; Kumaramanickavel G; Schürmann M; Mukkadan JK; Fernandez ST; John S; Weber JL; Denton MJ; Gal A
    Genomics; 1998 Mar; 48(3):341-5. PubMed ID: 9545639
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A gene for primary congenital glaucoma is not linked to the locus on chromosome 1q for autosomal dominant juvenile-onset open angle glaucoma.
    Anderson KL; Lewis RA; Bejjani BA; Baird L; Otterud B; Tomey KF; Astle WF; Dueker DK; Leppert M; Lupski JR
    J Glaucoma; 1996 Dec; 5(6):416-21. PubMed ID: 8946299
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15.
    Othmane KB; Johnson E; Menold M; Graham FL; Hamida MB; Hasegawa O; Rogala AD; Ohnishi A; Pericak-Vance M; Hentati F; Vance JM
    Genomics; 1999 Dec; 62(3):344-9. PubMed ID: 10644431
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping.
    Nürnberg G; Jacobi FK; Broghammer M; Becker C; Blin N; Nürnberg P; Stephani U; Pusch CM
    Int J Mol Med; 2008 Apr; 21(4):429-38. PubMed ID: 18360688
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Exclusion of TIMP3 as a candidate locus in age-related macular degeneration.
    De La Paz MA; Pericak-Vance MA; Lennon F; Haines JL; Seddon JM
    Invest Ophthalmol Vis Sci; 1997 May; 38(6):1060-5. PubMed ID: 9152225
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Exclusion of the cone-specific alpha-subunit of the transducin gene in Stargardt's disease.
    Gerber S; Rozet JM; Bonneau D; Souied E; Weissenbach J; Frezal J; Munnich A; Kaplan J
    Hum Genet; 1995 Apr; 95(4):382-4. PubMed ID: 7705831
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [A special form of Stargardt's disease/fundus flavimaculatus].
    Suzuki R; Hirose T
    Nippon Ganka Gakkai Zasshi; 1996 Jul; 100(7):562-7. PubMed ID: 8741342
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Stargardt's incipient flavimaculatus disease (apropos of 2 cases of pure fundus flavimaculatus)].
    Puech B; Turut P; François P; Hache JC
    Bull Soc Ophtalmol Fr; 1976; 76(7-8):739-44. PubMed ID: 1029569
    [No Abstract]   [Full Text] [Related]  

  • 35. A gene for achondroplasia-hypochondroplasia maps to chromosome 4p.
    Le Merrer M; Rousseau F; Legeai-Mallet L; Landais JC; Pelet A; Bonaventure J; Sanak M; Weissenbach J; Stoll C; Munnich A
    Nat Genet; 1994 Mar; 6(3):318-21. PubMed ID: 8012398
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Stargardt disease: linkage to the ABCR gene region on 1p21-p22 in Scandinavian families.
    Arnell H; Mäntyjärvi M; Tuppurainen K; Andréasson S; Dahl N
    Acta Ophthalmol Scand; 1998 Dec; 76(6):649-52. PubMed ID: 9881544
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The electroretinogram in Stargardt's disease and fundus flavimaculatus.
    Lachapelle P; Little JM; Roy MS
    Doc Ophthalmol; 1989 Dec; 73(4):395-404. PubMed ID: 2637122
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Retinal function in Stargardt's disease and fundus flavimaculatus.
    Moloney JB; Mooney DJ; O'Connor MA
    Am J Ophthalmol; 1983 Jul; 96(1):57-65. PubMed ID: 6869480
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Fundus flavimaculatus of dominant heredity (apropos of 2 families). Nosological considerations on Stargardt's disease].
    Turut P; Puech B; François P; Hache JC
    Bull Soc Ophtalmol Fr; 1975 Mar; 75(3):309-15. PubMed ID: 1204180
    [No Abstract]   [Full Text] [Related]  

  • 40. Linkage of the gene for cystinosis to markers on the short arm of chromosome 17. The Cystinosis Collaborative Research Group.
    Nat Genet; 1995 Jun; 10(2):246-8. PubMed ID: 7663525
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.