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Journal Abstract Search

177 related items for PubMed ID: 10507729

  • 1. Autosomal recessive retinitis pigmentosa locus RP28 maps between D2S1337 and D2S286 on chromosome 2p11-p15 in an Indian family.
    Gu S, Kumaramanickavel G, Srikumari CR, Denton MJ, Gal A.
    J Med Genet; 1999 Sep; 36(9):705-7. PubMed ID: 10507729
    [Abstract] [Full Text] [Related]

  • 2. Confirmation of linkage and refinement of the RP28 locus for autosomal recessive retinitis pigmentosa on chromosome 2p14-p15 in an Indian family.
    Kumar A, Shetty J, Kumar B, Blanton SH.
    Mol Vis; 2004 Jun 15; 10():399-402. PubMed ID: 15215745
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  • 3. 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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  • 4. 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 15; 42(7):1436-8. PubMed ID: 11381043
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  • 5. 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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  • 6. Evidence for a new locus for X-linked retinitis pigmentosa (RP23).
    Hardcastle AJ, Thiselton DL, Zito I, Ebenezer N, Mah TS, Gorin MB, Bhattacharya SS.
    Invest Ophthalmol Vis Sci; 2000 Jul 17; 41(8):2080-6. PubMed ID: 10892847
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  • 7. Linkage validation of RP25 Using the 10K genechip array and further refinement of the locus by new linked families.
    Barragán I, Abd El-Aziz MM, Borrego S, El-Ashry MF, O'Driscoll C, Bhattacharya SS, Antiñolo G.
    Ann Hum Genet; 2008 Jul 17; 72(Pt 4):454-62. PubMed ID: 18510647
    [Abstract] [Full Text] [Related]

  • 8. Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3.
    Banerjee P, Lewis CA, Kleyn PW, Shugart YY, Ross BM, Penchaszadeh GK, Ott J, Jacobson SG, Gilliam TC, Knowles JA.
    Genomics; 1998 Mar 01; 48(2):171-7. PubMed ID: 9521870
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  • 9. A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene.
    Jain PK, Lalwani AK, Li XC, Singleton TL, Smith TN, Chen A, Deshmukh D, Verma IC, Smith RJ, Wilcox ER.
    Genomics; 1998 Jun 01; 50(2):290-2. PubMed ID: 9653658
    [Abstract] [Full Text] [Related]

  • 10. CORD9 a new locus for arCRD: mapping to 8p11, estimation of frequency, evaluation of a candidate gene.
    Danciger M, Hendrickson J, Lyon J, Toomes C, McHale JC, Fishman GA, Inglehearn CF, Jacobson SG, Farber DB.
    Invest Ophthalmol Vis Sci; 2001 Oct 01; 42(11):2458-65. PubMed ID: 11581183
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  • 13. Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneity.
    Kwitek-Black AE, Carmi R, Duyk GM, Buetow KH, Elbedour K, Parvari R, Yandava CN, Stone EM, Sheffield VC.
    Nat Genet; 1993 Dec 01; 5(4):392-6. PubMed ID: 8298649
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  • 16. 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 01; 46(7):2264-70. PubMed ID: 15980210
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  • 17. Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q.
    Jordan SA, Farrar GJ, Kenna P, Humphries MM, Sheils DM, Kumar-Singh R, Sharp EM, Soriano N, Ayuso C, Benitez J.
    Nat Genet; 1993 May 01; 4(1):54-8. PubMed ID: 8513324
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  • 18. Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4.
    Tlili A, Masmoudi S, Dhouib H, Bouaziz S, Rebeh IB, Chouchen J, Turki K, Benzina Z, Charfedine I, Drira M, Ayadi H.
    Ann Hum Genet; 2007 Mar 01; 71(Pt 2):271-5. PubMed ID: 17166180
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  • 20. Identification of candidate regions for a novel Usher syndrome type II locus.
    Ben Rebeh I, Benzina Z, Dhouib H, Hadjamor I, Amyere M, Ayadi L, Turki K, Hammami B, Kmiha N, Kammoun H, Hakim B, Charfedine I, Vikkula M, Ghorbel A, Ayadi H, Masmoudi S.
    Mol Vis; 2008 Sep 19; 14():1719-26. PubMed ID: 18806881
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