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Journal Abstract Search

144 related items for PubMed ID: 8086748

  • 1. [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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  • 2. 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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  • 9. Retinitis pigmentosa in Puerto Rico.
    Tous HM, Izquierdo NJ.
    P R Health Sci J; 2006 Dec; 25(4):315-8. PubMed ID: 17550097
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  • 10. Problems in detecting etiological heterogeneity in genetic disease illustrated with retinitis pigmentosa.
    Beaty TH, Boughman JA.
    Am J Med Genet; 1986 Jul; 24(3):493-504. PubMed ID: 3728568
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  • 11. Assessment of clinical variables and counseling needs in patients with retinitis pigmentosa.
    Boughman JA, Caldwell RJ.
    Am J Med Genet; 1982 Jun; 12(2):185-93. PubMed ID: 7102723
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  • 12. Retinitis pigmentosa genetics: a study in Indian population.
    Vinchurkar MS, Sathye SM, Dikshit M.
    Indian J Ophthalmol; 1996 Jun; 44(2):77-82. PubMed ID: 8916593
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  • 13. [The incidence of Usher's syndrome and its clinical types].
    Bereketoğlu M, Avşar EU, Turan O, Afrashi F, Apaydin F.
    Kulak Burun Bogaz Ihtis Derg; 2002 Jun; 9(1):15-20. PubMed ID: 12122620
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  • 16. Retinitis pigmentosa in Ontario - a survey.
    Macrae WG.
    Birth Defects Orig Artic Ser; 1982 Jun; 18(6):175-85. PubMed ID: 7171753
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  • 17. Is there genetic heterogeneity in Usher's syndrome?
    Matthews TW, Poliquin J, Mount J, MacFie D.
    J Otolaryngol; 1987 Mar; 16(2):61-6. PubMed ID: 3599157
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  • 18. Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families.
    Riazuddin SA, Zulfiqar F, Zhang Q, Sergeev YV, Qazi ZA, Husnain T, Caruso R, Riazuddin S, Sieving PA, Hejtmancik JF.
    Invest Ophthalmol Vis Sci; 2005 Jul; 46(7):2264-70. PubMed ID: 15980210
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  • 19. Nonsyndromic retinitis pigmentosa is highly prevalent in the Jerusalem region with a high frequency of founder mutations.
    Sharon D, Banin E.
    Mol Vis; 2015 Jul; 21():783-92. PubMed ID: 26261414
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  • 20. A new clinical classification for Usher's syndrome based on a new subtype of Usher's syndrome type I.
    Otterstedde CR, Spandau U, Blankenagel A, Kimberling WJ, Reisser C.
    Laryngoscope; 2001 Jan; 111(1):84-6. PubMed ID: 11192904
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