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Journal Abstract Search

72 related items for PubMed ID: 5173138

  • 1. 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
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  • 5. [Hereditary maculopathy in typical retinitis pigmentosa. Apropos of 40 cases].
    Chachia N, Romdane K, Zaghdane M, Hadj Hamida FB, Khayrallah M, Haddad M.
    Ophtalmologie; 1989 Mar; 3(1):67-8. PubMed ID: 2641075
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  • 8. 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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  • 10. Autosomal recessive inheritance in 'senile' retinitis pigmentosa.
    Grøndahl J.
    Acta Ophthalmol (Copenh); 1987 Apr; 65(2):231-6. PubMed ID: 3604615
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  • 11. CLRN1 mutations cause nonsyndromic retinitis pigmentosa.
    Khan MI, Kersten FF, Azam M, Collin RW, Hussain A, Shah ST, Keunen JE, Kremer H, Cremers FP, Qamar R, den Hollander AI.
    Ophthalmology; 2011 Jul; 118(7):1444-8. PubMed ID: 21310491
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  • 12. [Autosomal recessive hereditary type of pigmentary degeneration of the retina].
    Ondrejcák M, Michalíková E.
    Cesk Oftalmol; 1976 Mar; 32(2):142-4. PubMed ID: 1268993
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  • 13. Cleft lip and cone-rod dystrophy in a consanguineous sibship.
    Ausems MG, Wittebol-Post D, Hennekam RC.
    Clin Dysmorphol; 1996 Oct; 5(4):307-11. PubMed ID: 8905195
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  • 14. 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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  • 15. Novel RDH5 mutation in family with mother having fundus albipunctatus and three children with retinitis pigmentosa.
    Wang C, Nakanishi N, Ohishi K, Hikoya A, Koide K, Sato M, Nakamura M, Hotta Y, Minoshima S.
    Ophthalmic Genet; 2008 Mar; 29(1):29-32. PubMed ID: 18363170
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  • 17. Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3.
    Finckh U, Xu S, Kumaramanickavel G, Schürmann M, Mukkadan JK, Fernandez ST, John S, Weber JL, Denton MJ, Gal A.
    Genomics; 1998 Mar 15; 48(3):341-5. PubMed ID: 9545639
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  • 18. A family with retinitis pigmentosa and ESRD with late presentation, hypertension and absence of polyuria or salt wasting.
    Friedlaender MM, Rubinger D, Silver J, Zlotogora J, Merin S, Popovtzer MM.
    Clin Nephrol; 1986 Apr 15; 25(4):202-6. PubMed ID: 3698352
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