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162 related items for PubMed ID: 10509675

  • 21. Mapping of putative ether-anesthesia resistance gene using C57BL/6J and MSM/Ms mouse strains.
    Megumi T, Song CW, Park YG, Tanaka Y, Uchida I, Okumoto M.
    J Anesth; 2004; 18(4):267-76. PubMed ID: 15549469
    [Abstract] [Full Text] [Related]

  • 22. A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13.
    Hameed A, Khaliq S, Ismail M, Anwar K, Ebenezer ND, Jordan T, Mehdi SQ, Payne AM, Bhattacharya SS.
    Invest Ophthalmol Vis Sci; 2000 Mar; 41(3):629-33. PubMed ID: 10711674
    [Abstract] [Full Text] [Related]

  • 23. Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28.
    Villard L, des Portes V, Levy N, Louboutin JP, Recan D, Coquet M, Chabrol B, Figarella-Branger D, Chelly J, Pellissier JF, Fontes M.
    Eur J Hum Genet; 2000 Feb; 8(2):125-9. PubMed ID: 10757644
    [Abstract] [Full Text] [Related]

  • 24. Mapping of the X-linked cataract (Xcat) mutation, the gene implicated in the Nance Horan syndrome, on the mouse X chromosome.
    Stambolian D, Favor J, Silvers W, Avner P, Chapman V, Zhou E.
    Genomics; 1994 Jul 15; 22(2):377-80. PubMed ID: 7806224
    [Abstract] [Full Text] [Related]

  • 25. Fine mapping of the circling (cir) gene on the distal portion of mouse chromosome 9.
    Cho KI, Lee JW, Kim KS, Lee EJ, Suh JG, Lee HJ, Kim HT, Hong SH, Chung WH, Chang KT, Hyun BH, Oh YS, Ryoo ZY.
    Comp Med; 2003 Dec 15; 53(6):642-8. PubMed ID: 14727813
    [Abstract] [Full Text] [Related]

  • 26. Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescens.
    Hawes NL, Chang B, Hageman GS, Nusinowitz S, Nishina PM, Schneider BS, Smith RS, Roderick TH, Davisson MT, Heckenlively JR.
    Invest Ophthalmol Vis Sci; 2000 Sep 15; 41(10):3149-57. PubMed ID: 10967077
    [Abstract] [Full Text] [Related]

  • 27. [Clinical features and genetic analysis in a family with X-linked incomplete congenital stationary night blindness (CSNBi)].
    Schmitt-Bernard CF, Bareil C, Hamel CP, Beaufrere L, Arnaud B, Claustres M, de Meeus A.
    J Fr Ophtalmol; 1998 Apr 15; 21(4):251-6. PubMed ID: 9759413
    [Abstract] [Full Text] [Related]

  • 28. Development of a 1.4-Mb BAC/PAC contig and physical map within the critical region for complete X-linked congenital stationary night blindness in Xp11.4.
    Sparkes RL, Summer CG, Boycott KM, Zahorchak RJ, Bech-Hansen NT.
    Genomics; 2000 Aug 15; 68(1):97-100. PubMed ID: 10950933
    [Abstract] [Full Text] [Related]

  • 29. Localization of a prostate cancer predisposition gene to an 880-kb region on chromosome 22q12.3 in Utah high-risk pedigrees.
    Camp NJ, Farnham JM, Cannon-Albright LA.
    Cancer Res; 2006 Oct 15; 66(20):10205-12. PubMed ID: 17047086
    [Abstract] [Full Text] [Related]

  • 30. Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian family.
    Rozzo C, Fossarello M, Galleri G, Miano MG, Ciccodicola A, Sole G, Pirastu M.
    Eur J Hum Genet; 1999 Jul 15; 7(5):574-8. PubMed ID: 10439964
    [Abstract] [Full Text] [Related]

  • 31. A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26.
    McAuley EZ, Blair IP, Liu Z, Fullerton JM, Scimone A, Van Herten M, Evans MR, Kirkby KC, Donald JA, Mitchell PB, Schofield PR.
    Mol Psychiatry; 2009 May 15; 14(5):492-500. PubMed ID: 18227837
    [Abstract] [Full Text] [Related]

  • 32. A dominant form of congenital stationary night blindness (adCSNB) in a large Chinese family.
    Liu X, Zhuang S, Hu S, Zhang F, Lin B, Li X, Xu D, Chen SH.
    Ann Hum Genet; 2005 May 15; 69(Pt 3):315-21. PubMed ID: 15845035
    [Abstract] [Full Text] [Related]

  • 33. Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7.
    Bech-Hansen NT, Moore BJ, Pearce WG.
    Genomics; 1992 Feb 15; 12(2):409-11. PubMed ID: 1740347
    [Abstract] [Full Text] [Related]

  • 34. Genetic linkage of snowflake vitreoretinal degeneration to chromosome 2q36.
    Jiao X, Ritter R, Hejtmancik JF, Edwards AO.
    Invest Ophthalmol Vis Sci; 2004 Dec 15; 45(12):4498-503. PubMed ID: 15557460
    [Abstract] [Full Text] [Related]

  • 35. A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosome.
    Bech-Hansen NT, Field LL, Schramm AM, Reedyk M, Craig IW, Fraser NJ, Pearce WG.
    Hum Genet; 1990 Apr 15; 84(5):406-8. PubMed ID: 1969841
    [Abstract] [Full Text] [Related]

  • 36. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.
    Br J Dermatol; 2005 Jan 15; 152(1):29-36. PubMed ID: 15656797
    [Abstract] [Full Text] [Related]

  • 37.
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  • 38. An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.
    Strom TM, Nyakatura G, Apfelstedt-Sylla E, Hellebrand H, Lorenz B, Weber BH, Wutz K, Gutwillinger N, Rüther K, Drescher B, Sauer C, Zrenner E, Meitinger T, Rosenthal A, Meindl A.
    Nat Genet; 1998 Jul 15; 19(3):260-3. PubMed ID: 9662399
    [Abstract] [Full Text] [Related]

  • 39. A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder.
    Littink KW, van Genderen MM, Collin RW, Roosing S, de Brouwer AP, Riemslag FC, Venselaar H, Thiadens AA, Hoyng CB, Rohrschneider K, den Hollander AI, Cremers FP, van den Born LI.
    Invest Ophthalmol Vis Sci; 2009 May 15; 50(5):2344-50. PubMed ID: 19074807
    [Abstract] [Full Text] [Related]

  • 40. Hereditary keratoconus-like keratopathy in Japanese wild mice mapped to mouse Chromosome 13.
    Tachibana M, Okamoto M, Sakamoto M, Matsushima Y.
    Mamm Genome; 2002 Dec 15; 13(12):692-5. PubMed ID: 12514747
    [Abstract] [Full Text] [Related]

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