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Journal Abstract Search

305 related items for PubMed ID: 9135384

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  • 2. Autosomal dominant retinitis pigmentosa: localization of a disease gene (RP6) to the short arm of chromosome 6.
    Farrar GJ, Jordan SA, Kenna P, Humphries MM, Kumar-Singh R, McWilliam P, Allamand V, Sharp E, Humphries P.
    Genomics; 1991 Dec; 11(4):870-4. PubMed ID: 1783395
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  • 6. Gene of type II autosomal dominant retinitis pigmentosa maps on the long arm of chromosome 3.
    Olsson JE, Samanns C, Jimenez J, Pongratz J, Chand A, Watty A, Seuchter SA, Denton M, Gal A.
    Am J Med Genet; 1990 Apr; 35(4):595-9. PubMed ID: 2333895
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  • 7. Autosomal dominant retinitis pigmentosa locus on chromosome 19q in a Japanese family.
    Xu S, Nakazawa M, Tamai M, Gal A.
    J Med Genet; 1995 Nov; 32(11):915-6. PubMed ID: 8592343
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  • 8. Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3.
    McWilliam P, Farrar GJ, Kenna P, Bradley DG, Humphries MM, Sharp EM, McConnell DJ, Lawler M, Sheils D, Ryan C.
    Genomics; 1989 Oct; 5(3):619-22. PubMed ID: 2613244
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  • 9. Autosomal dominant retinitis pigmentosa (adRP): exclusion of a gene from three mapped loci provides evidence for the existence of a fourth locus.
    Jordan SA, del Rio T, Soriano N, Garcia-Sandoval B, Kenna P, Ayuso C, Benitez J, Humphries P.
    Hum Mol Genet; 1992 Sep; 1(6):411-5. PubMed ID: 1301915
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  • 10. Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: linkage mapping in a second, unrelated family.
    McGuire RE, Gannon AM, Sullivan LS, Rodriguez JA, Daiger SP.
    Hum Genet; 1995 Jan; 95(1):71-4. PubMed ID: 7814030
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  • 12. Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation.
    Zhang Q, Zulfiqar F, Riazuddin SA, Xiao X, Ahmad Z, Riazuddin S, Hejtmancik JF.
    Mol Vis; 2004 Nov 17; 10():884-9. PubMed ID: 15570217
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  • 15. DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3.
    Khan SY, Riazuddin S, Shahzad M, Ahmed N, Zafar AU, Rehman AU, Morell RJ, Griffith AJ, Ahmed ZM, Riazuddin S, Friedman TB.
    Eur J Hum Genet; 2010 Jan 17; 18(1):125-9. PubMed ID: 19603065
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  • 18. Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the disease.
    Humphries P, Farrar GJ, Kenna P, McWilliam P.
    Clin Genet; 1990 Jul 17; 38(1):1-13. PubMed ID: 2201466
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  • 20. A novel locus (RP33) for autosomal dominant retinitis pigmentosa mapping to chromosomal region 2cen-q12.1.
    Zhao C, Lu S, Zhou X, Zhang X, Zhao K, Larsson C.
    Hum Genet; 2006 Jul 17; 119(6):617-23. PubMed ID: 16612614
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