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Journal Abstract Search

179 related items for PubMed ID: 3337193

  • 1. Cosegregation of X-linked retinitis pigmentosa and hemophilia A.
    Rabinowitz YS, Ladda RL, Sassani JW, Eyster ME.
    Am J Ophthalmol; 1988 Jan 15; 105(1):46-56. PubMed ID: 3337193
    [Abstract] [Full Text] [Related]

  • 2. X-linked retinitis pigmentosa associated with a 2-base pair insertion in codon 99 of the RP3 gene RPGR.
    Weleber RG, Butler NS, Murphey WH, Sheffield VC, Stone EM.
    Arch Ophthalmol; 1997 Nov 15; 115(11):1429-35. PubMed ID: 9366675
    [Abstract] [Full Text] [Related]

  • 3. X-linked recessive retinitis pigmentosa. Clinical characteristics of carriers.
    Fishman GA, Weinberg AB, McMahon TT.
    Arch Ophthalmol; 1986 Sep 15; 104(9):1329-35. PubMed ID: 3753283
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  • 4. Variable expressivity in a Japanese family with autosomal dominant retinitis pigmentosa closely linked to chromosome 19q.
    Nakazawa M, Xu S, Gal A, Wada Y, Tamai M.
    Arch Ophthalmol; 1996 Mar 15; 114(3):318-22. PubMed ID: 8600893
    [Abstract] [Full Text] [Related]

  • 5. Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene.
    Andréasson S, Ponjavic V, Abrahamson M, Ehinger B, Wu W, Fujita R, Buraczynska M, Swaroop A.
    Am J Ophthalmol; 1997 Jul 15; 124(1):95-102. PubMed ID: 9222238
    [Abstract] [Full Text] [Related]

  • 6. A longitudinal study of visual function in carriers of X-linked recessive retinitis pigmentosa.
    Grover S, Fishman GA, Anderson RJ, Lindeman M.
    Ophthalmology; 2000 Feb 15; 107(2):386-96. PubMed ID: 10690843
    [Abstract] [Full Text] [Related]

  • 7. X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60.
    Fishman GA, Grover S, Jacobson SG, Alexander KR, Derlacki DJ, Wu W, Buraczynska M, Swaroop A.
    Ophthalmology; 1998 Dec 15; 105(12):2286-96. PubMed ID: 9855162
    [Abstract] [Full Text] [Related]

  • 8. A new 2-base pair deletion in the RPGR gene in a black family with X-linked retinitis pigmentosa.
    Fishman GA, Grover S, Buraczynska M, Wu W, Swaroop A.
    Arch Ophthalmol; 1998 Feb 15; 116(2):213-8. PubMed ID: 9488274
    [Abstract] [Full Text] [Related]

  • 9. Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype.
    Ponjavic V, Andréasson S, Abrahamson M, Ehinger B, Gieser L, Fujita R, Swaroop A.
    Ophthalmic Genet; 1998 Dec 15; 19(4):187-96. PubMed ID: 9895243
    [Abstract] [Full Text] [Related]

  • 10. X-linked retinitis pigmentosa.
    Bird AC.
    Br J Ophthalmol; 1975 Apr 15; 59(4):177-99. PubMed ID: 1138842
    [Abstract] [Full Text] [Related]

  • 11. X-linked retinitis pigmentosa.
    Jay B, Bird A.
    Trans Am Acad Ophthalmol Otolaryngol; 1973 Apr 15; 77(5):OP641-51. PubMed ID: 4784907
    [No Abstract] [Full Text] [Related]

  • 12. Clinical and electrophysiological observations on genetic carriers of retinitis pigmentosa in a family (pedigree Tt) showing sex-linked inheritance.
    Imaizumi K, Takahashi R, Tazawa Y, Yamada K, Mita K.
    Adv Exp Med Biol; 1972 Apr 15; 24(0):301-7. PubMed ID: 4671885
    [No Abstract] [Full Text] [Related]

  • 13. Comparison of intraocular light scatter in carriers of choroideremia and X-linked retinitis pigmentosa.
    Grover S, Alexander KR, Fishman GA, Ryan J.
    Ophthalmology; 2002 Jan 15; 109(1):159-63. PubMed ID: 11772598
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  • 20. Electroretinographic testing as an aid in detection of carriers of X-chromosome-linked retinitis pigmentosa.
    Berson EL, Rosen JB, Simonoff EA.
    Am J Ophthalmol; 1979 Apr 15; 87(4):460-8. PubMed ID: 443310
    [Abstract] [Full Text] [Related]

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