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 *

137 related articles for article (PubMed ID: 1427834)

  • 1. Linkage analysis in X-linked congenital stationary night blindness.
    Aldred MA; Dry KL; Sharp DM; Van Dorp DB; Brown J; Hardwick LJ; Lester DH; Pryde FE; Teague PW; Jay M
    Genomics; 1992 Sep; 14(1):99-104. PubMed ID: 1427834
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3.
    Musarella MA; Weleber RG; Murphey WH; Young RS; Anson-Cartwright L; Mets M; Kraft SP; Polemeno R; Litt M; Worton RG
    Genomics; 1989 Nov; 5(4):727-37. PubMed ID: 2574143
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7.
    Bech-Hansen NT; Moore BJ; Pearce WG
    Genomics; 1992 Feb; 12(2):409-11. PubMed ID: 1740347
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23.
    Bech-Hansen NT; Boycott KM; Gratton KJ; Ross DA; Field LL; Pearce WG
    Hum Genet; 1998 Aug; 103(2):124-30. PubMed ID: 9760193
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Evidence for genetic heterogeneity in X-linked congenital stationary night blindness.
    Boycott KM; Pearce WG; Musarella MA; Weleber RG; Maybaum TA; Birch DG; Miyake Y; Young RS; Bech-Hansen NT
    Am J Hum Genet; 1998 Apr; 62(4):865-75. PubMed ID: 9529339
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Complete form of X-linked congenital stationary night blindness: refined mapping and evidence of genetic homogeneity.
    Pusch CM; Maurer J; Ramser J; Tomiuk J; Achatz H; Pesch K; Lichtner P; Apfelstedt-Sylla E; Jacobi FK; Berger W; Meindl A; Wissinger B
    Int J Mol Med; 2001 Feb; 7(2):155-61. PubMed ID: 11172618
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Linkage analysis in a Dutch family with X-linked recessive congenital stationary night blindness (XL-CSNB).
    Berger W; van Duijnhoven G; Pinckers A; Smits A; Ropers HH; Cremers F
    Hum Genet; 1995 Jan; 95(1):67-70. PubMed ID: 7814029
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
    Bech-Hansen NT; Naylor MJ; Maybaum TA; Pearce WG; Koop B; Fishman GA; Mets M; Musarella MA; Boycott KM
    Nat Genet; 1998 Jul; 19(3):264-7. PubMed ID: 9662400
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Manifestations of X-linked congenital stationary night blindness in three daughters of an affected male: demonstration of homozygosity.
    Bech-Hansen NT; Pearce WG
    Am J Hum Genet; 1993 Jan; 52(1):71-7. PubMed ID: 8434607
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosome.
    Bech-Hansen NT; Field LL; Schramm AM; Reedyk M; Craig IW; Fraser NJ; Pearce WG
    Hum Genet; 1990 Apr; 84(5):406-8. PubMed ID: 1969841
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian family.
    Rozzo C; Fossarello M; Galleri G; Miano MG; Ciccodicola A; Sole G; Pirastu M
    Eur J Hum Genet; 1999 Jul; 7(5):574-8. PubMed ID: 10439964
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Linkage analysis in a family with complete type congenital stationary night blindness with and without myopia.
    Dry KL; Van Dorp DB; Aldred MA; Brown J; Hardwick LJ; Wright AF
    Clin Genet; 1993 May; 43(5):250-4. PubMed ID: 8375106
    [TBL] [Abstract][Full Text] [Related]  

  • 13. GNAT1 associated with autosomal recessive congenital stationary night blindness.
    Naeem MA; Chavali VR; Ali S; Iqbal M; Riazuddin S; Khan SN; Husnain T; Sieving PA; Ayyagari R; Riazuddin S; Hejtmancik JF; Riazuddin SA
    Invest Ophthalmol Vis Sci; 2012 Mar; 53(3):1353-61. PubMed ID: 22190596
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F.
    Boycott KM; Pearce WG; Bech-Hansen NT
    Can J Ophthalmol; 2000 Jun; 35(4):204-13. PubMed ID: 10900517
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp.
    Gal A; Schinzel A; Orth U; Fraser NA; Mollica F; Craig IW; Kruse T; Mächler M; Neugebauer M; Bleeker-Wagemakers LM
    Hum Genet; 1989 Mar; 81(4):315-8. PubMed ID: 2564836
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1.
    Jacobi FK; Broghammer M; Pesch K; Zrenner E; Berger W; Meindl A; Pusch CM
    Hum Genet; 2000 Jul; 107(1):89-91. PubMed ID: 10982042
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Electrophysiologic tests for diagnosis of congenital night blindness].
    Lubiński W; Palacz A; Penkala K; Palacz O
    Klin Oczna; 1996 Jan; 98(1):9-12. PubMed ID: 9019583
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Variable expressivity in X-linked congenital stationary night blindness.
    Pearce WG; Reedyk M; Coupland SG
    Can J Ophthalmol; 1990 Feb; 25(1):3-10. PubMed ID: 2328435
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Localization of CSNBX (CSNB4) between the retinitis pigmentosa loci RP2 and RP3 on proximal Xp.
    Hardcastle AJ; David-Gray ZK; Jay M; Bird AC; Bhattacharya SS
    Invest Ophthalmol Vis Sci; 1997 Dec; 38(13):2750-5. PubMed ID: 9418727
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Aland eye disease: linkage data.
    Schwartz M; Rosenberg T
    Genomics; 1991 Jun; 10(2):327-32. PubMed ID: 2071141
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.