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PUBMED FOR HANDHELDS

Journal Abstract Search

132 related items for PubMed ID: 1424244

  • 21. Retinitis pigmentosa, autosomal recessive type: three kindreds.
    Schleutermann D, Pierce E, Cantolino SJ, Naidoff M.
    Birth Defects Orig Artic Ser; 1971 Mar; 7(3):180-2. PubMed ID: 5173138
    [No Abstract] [Full Text] [Related]

  • 22. [Cochleo-vestibular manifestations in retinitis pigmentosa (Usher's syndrome)].
    Torres G, Kume M, Corvera J, Prado A.
    Acta Otorinolaryngol Iber Am; 1972 Mar; 23(4):517-24. PubMed ID: 4539456
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  • 28. A survey of hereditary aspects of pigmentary retinal dystrophies.
    Dickinson P, Mulhall L.
    Aust N Z J Ophthalmol; 1989 Aug; 17(3):247-56. PubMed ID: 2803770
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  • 29. Autosomal dominantly inherited retinitis pigmentosa with a severe clinical course.
    Satheesh P, Chacko A, Rajan GV.
    J Assoc Physicians India; 1993 Nov; 41(11):756. PubMed ID: 8005942
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  • 32. Retinal manifestations in familial juvenile nephronophthisis.
    Godel V, Iaina A, Nemet P, Lazar M.
    Clin Genet; 1979 Oct; 16(4):277-81. PubMed ID: 519897
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  • 34. A syndrome with retinitis pigmentosa, progressive hearing impairment, vestibular dysfunction, and congenital cataract.
    Rosenberg T, Parving A.
    Acta Ophthalmol Scand Suppl; 1996 Oct; (219):50-3. PubMed ID: 8741120
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  • 35. [An epidemiogenetic study of typical retinitis pigmentosa in Japan--a preliminary report of nationwide, multicenter study].
    Fujiki K, Hayakawa M, Kanai A, Matsumura M, Koizumi H, Tamai M, Shiono T, Tokoro T, Akazawa Y, Kubota N.
    Nippon Ganka Gakkai Zasshi; 1992 Feb; 96(2):225-30. PubMed ID: 1558019
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  • 36. Novel homozygous mutation in the alpha subunit of the rod cGMP gated channel (CNGA1) in two Spanish sibs affected with autosomal recessive retinitis pigmentosa.
    Paloma E, Martínez-Mir A, García-Sandoval B, Ayuso C, Vilageliu L, Gonzàlez-Duarte R, Balcells S.
    J Med Genet; 2002 Oct; 39(10):E66. PubMed ID: 12362048
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  • 37. An evaluation of genetic carriers of Usher's syndrome.
    Holland MG, Cambie E, Kloepfer W.
    Am J Ophthalmol; 1972 Nov; 74(5):940-7. PubMed ID: 4539460
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  • 38. A new locus for autosomal recessive RP (RP29) mapping to chromosome 4q32-q34 in a Pakistani family.
    Hameed A, Khaliq S, Ismail M, Anwar K, Mehdi SQ, Bessant D, Payne AM, Bhattacharya SS.
    Invest Ophthalmol Vis Sci; 2001 Jun; 42(7):1436-8. PubMed ID: 11381043
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