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 *

132 related articles for article (PubMed ID: 6803203)

  • 21. Gene of type II autosomal dominant retinitis pigmentosa maps on the long arm of chromosome 3.
    Olsson JE; Samanns C; Jimenez J; Pongratz J; Chand A; Watty A; Seuchter SA; Denton M; Gal A
    Am J Med Genet; 1990 Apr; 35(4):595-9. PubMed ID: 2333895
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A new family linked to the RP13 locus for autosomal dominant retinitis pigmentosa on distal 17p.
    Tarttelin EE; Plant C; Weissenbach J; Bird AC; Bhattacharya SS; Inglehearn CF
    J Med Genet; 1996 Jun; 33(6):518-20. PubMed ID: 8782056
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19.
    al-Maghtheh M; Inglehearn CF; Keen TJ; Evans K; Moore AT; Jay M; Bird AC; Bhattacharya SS
    Hum Mol Genet; 1994 Feb; 3(2):351-4. PubMed ID: 8004108
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p.
    Inglehearn CF; Carter SA; Keen TJ; Lindsey J; Stephenson AM; Bashir R; al-Maghtheh M; Moore AT; Jay M; Bird AC
    Nat Genet; 1993 May; 4(1):51-3. PubMed ID: 8513323
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Further evidence of exclusion of linkage between type II autosomal dominant retinitis pigmentosa (ADRP) and D3S47 on 3q.
    Blanton SH; Cottingham AW; Giesenschlag N; Heckenlively JR; Humphries P; Daiger SP
    Genomics; 1990 Sep; 8(1):179-81. PubMed ID: 2081594
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Retinitis pigmentosa, AD type I: exclusion of linkage to D3S47 (C17) in a large South African family of British origin.
    Greenberg J; Babaya M; Ramesar R; Beighton P
    Clin Genet; 1992 Jun; 41(6):322-5. PubMed ID: 1623630
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q.
    Jordan SA; Farrar GJ; Kenna P; Humphries MM; Sheils DM; Kumar-Singh R; Sharp EM; Soriano N; Ayuso C; Benitez J
    Nat Genet; 1993 May; 4(1):54-8. PubMed ID: 8513324
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Autosomal recessive retinitis pigmentosa locus RP28 maps between D2S1337 and D2S286 on chromosome 2p11-p15 in an Indian family.
    Gu S; Kumaramanickavel G; Srikumari CR; Denton MJ; Gal A
    J Med Genet; 1999 Sep; 36(9):705-7. PubMed ID: 10507729
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Evidence for further genetic heterogeneity in autosomal dominant retinitis pigmentosa.
    Kumar-Singh R; Kenna PF; Farrar GJ; Humphries P
    Genomics; 1993 Jan; 15(1):212-5. PubMed ID: 8432539
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Linkage between the X-linked retinitis pigmentosa locus and the L1.28 locus.
    Mukai S; Dryja TP; Bruns GA; Aldridge JF; Berson EL
    Am J Ophthalmol; 1985 Aug; 100(2):225-9. PubMed ID: 4025464
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Exclusion of linkage between D3S47 (C17) and ADRPII gene in two large families of moderate autosomal dominant retinitis pigmentosa: evidence for genetic heterogeneity.
    Kaplan J; Guasconi G; Dufier JL; Michel-Awad A; David A; Munnich A; Frezal J
    Ann Genet; 1990; 33(3):152-4. PubMed ID: 2288459
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele.
    McGee TL; Devoto M; Ott J; Berson EL; Dryja TP
    Am J Hum Genet; 1997 Nov; 61(5):1059-66. PubMed ID: 9345108
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness.
    Kenna P; Mansergh F; Millington-Ward S; Erven A; Kumar-Singh R; Brennan R; Farrar GJ; Humphries P
    Br J Ophthalmol; 1997 Mar; 81(3):207-13. PubMed ID: 9135384
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A novel 7 bp deletion in PRPF31 associated with autosomal dominant retinitis pigmentosa with incomplete penetrance in an Indian family.
    Saini S; Robinson PN; Singh JR; Vanita V
    Exp Eye Res; 2012 Nov; 104():82-8. PubMed ID: 23041261
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Refined mapping of the gene for autosomal dominant retinitis pigmentosa (RP17) on chromosome 17q22.
    den Hollander AI; van der Velde-Visser SD; Pinckers AJ; Hoyng CB; Brunner HG; Cremers FP
    Hum Genet; 1999 Jan; 104(1):73-6. PubMed ID: 10071195
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14.
    Wright AF; Bhattacharya SS; Clayton JF; Dempster M; Tippett P; McKeown CM; Jay M; Jay B; Bird AC
    Am J Hum Genet; 1987 Oct; 41(4):635-44. PubMed ID: 3477957
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 loci.
    Aldred MA; Teague PW; Jay M; Bundey S; Redmond RM; Jay B; Bird AC; Bhattacharya SS; Wright AF
    J Med Genet; 1994 Nov; 31(11):848-52. PubMed ID: 7853368
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of a Novel Gene on 10q22.1 Causing Autosomal Dominant Retinitis Pigmentosa (adRP).
    Daiger SP; Sullivan LS; Bowne SJ; Koboldt DC; Blanton SH; Wheaton DK; Avery CE; Cadena ED; Koenekoop RK; Fulton RS; Wilson RK; Weinstock GM; Lewis RA; Birch DG
    Adv Exp Med Biol; 2016; 854():193-200. PubMed ID: 26427411
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Localization of the gene for dominant cystoid macular dystrophy on chromosome 7p.
    Kremer H; Pinckers A; van den Helm B; Deutman AF; Ropers HH; Mariman EC
    Hum Mol Genet; 1994 Feb; 3(2):299-302. PubMed ID: 8004098
    [TBL] [Abstract][Full Text] [Related]  

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