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Journal Abstract Search

157 related items for PubMed ID: 9410231

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  • 3. [Distribution of the frequency of various Mendelian modes of inheritance in families with retinopathia pigmentosa. Results of an evaluation of the RP register of the Munster University Ophthalmology Clinic].
    Gerding H, Busse H.
    Ophthalmologe; 1994 Jun; 91(3):322-8. PubMed ID: 8086748
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  • 4. Prevalence of posterior subcapsular lens opacities in patients with retinitis pigmentosa.
    Fishman GA, Anderson RJ, Lourenco P.
    Br J Ophthalmol; 1985 Apr; 69(4):263-6. PubMed ID: 3994942
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  • 7. The frequency of posterior subcapsular cataract in the hereditary retinal degenerations.
    Heckenlively J.
    Am J Ophthalmol; 1982 Jun; 93(6):733-8. PubMed ID: 7091261
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  • 8. Epidemiology of retinitis pigmentosa in the Valencian community (Spain).
    Nájera C, Millán JM, Beneyto M, Prieto F.
    Genet Epidemiol; 1995 Jun; 12(1):37-46. PubMed ID: 7713399
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  • 11. Retinitis pigmentosa in Spain. The Spanish Multicentric and Multidisciplinary Group for Research into Retinitis Pigmentosa.
    Ayuso C, Garcia-Sandoval B, Najera C, Valverde D, Carballo M, Antiñolo G.
    Clin Genet; 1995 Sep; 48(3):120-2. PubMed ID: 8556816
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  • 12. Usher's syndrome type 3 in Finland.
    Pakarinen L, Karjalainen S, Simola KO, Laippala P, Kaitalo H.
    Laryngoscope; 1995 Jun; 105(6):613-7. PubMed ID: 7769945
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  • 13. Usher's syndrome, temporal bone pathology.
    Cremers CW, Delleman WJ.
    Int J Pediatr Otorhinolaryngol; 1988 Oct; 16(1):23-30. PubMed ID: 3203983
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  • 14. [Visual acuity and full-field electroretinography in patients with Usher's syndrome].
    Mendieta L, Berezovsky A, Salomão SR, Sacai PY, Pereira JM, Fantini SC.
    Arq Bras Oftalmol; 2005 Oct; 68(2):171-6. PubMed ID: 15905936
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  • 15. Hereditary and clinical features of retinitis pigmentosa in Koreans.
    Lee SH, Yu HG, Seo JM, Moon SW, Moon JW, Kim SJ, Chung H.
    J Korean Med Sci; 2010 Jun; 25(6):918-23. PubMed ID: 20514315
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  • 17. Multicenter genetic study of retinitis pigmentosa in Japan: I. Genetic heterogeneity in typical retinitis pigmentosa.
    Hayakawa M, Fujiki K, Kanai A, Matsumura M, Honda Y, Sakaue H, Tamai M, Sakuma T, Tokoro T, Yura T, Kubota N, Kawano S, Matsui M, Yuzawa M, Oguchi Y, Akeo K, Adachi E, Kimura T, Miyake Y, Horiguchi M, Wakabayashi K, Ishizaka N, Koizumi K, Uyama M, Ohba N.
    Jpn J Ophthalmol; 1997 Jun; 41(1):1-6. PubMed ID: 9147180
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  • 18. A study of retinitis pigmentosa in the City of Birmingham. II Clinical and genetic heterogeneity.
    Bundey S, Crews SJ.
    J Med Genet; 1984 Dec; 21(6):421-8. PubMed ID: 6512830
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  • 20. Prevalence of foveal lesions in type 1 and type 2 Usher's syndrome.
    Fishman GA, Anderson RJ, Lam BL, Derlacki DJ.
    Arch Ophthalmol; 1995 Jun; 113(6):770-3. PubMed ID: 7786220
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