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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

125 related items for PubMed ID: 15025575

  • 21.
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  • 23. Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping.
    Nürnberg G, Jacobi FK, Broghammer M, Becker C, Blin N, Nürnberg P, Stephani U, Pusch CM.
    Int J Mol Med; 2008 Apr; 21(4):429-38. PubMed ID: 18360688
    [Abstract] [Full Text] [Related]

  • 24. Mapping of plumage colour and blood protein loci on the microsatellite linkage map of the Japanese quail.
    Miwa M, Inoue-Murayama M, Kayang BB, Vignal A, Minvielle F, Monvoisin JL, Takahashi H, Ito S.
    Anim Genet; 2005 Oct; 36(5):396-400. PubMed ID: 16167982
    [Abstract] [Full Text] [Related]

  • 25. Genetic investigation of equine recurrent uveitis in Appaloosa horses.
    Rockwell H, Mack M, Famula T, Sandmeyer L, Bauer B, Dwyer A, Lassaline M, Beeson S, Archer S, McCue M, Bellone RR.
    Anim Genet; 2020 Feb; 51(1):111-116. PubMed ID: 31793009
    [Abstract] [Full Text] [Related]

  • 26. Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32.
    Wali A, Chishti M, Ayub M, Yasinzai M, Kafaitullah, Ali G, John P, Ahmad W.
    Clin Genet; 2007 Jul; 72(1):23-9. PubMed ID: 17594396
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  • 27. Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers.
    Masmoudi S, Charfedine I, Rebeh IB, Rebai A, Tlili A, Ghorbel AM, Belguith H, Petit C, Drira M, Ayadi H.
    Clin Genet; 2004 Oct; 66(4):358-64. PubMed ID: 15355440
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  • 28. Assignment of the horse grey coat colour gene to ECA25 using whole genome scanning.
    Swinburne JE, Hopkins A, Binns MM.
    Anim Genet; 2002 Oct; 33(5):338-42. PubMed ID: 12354141
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  • 29. Genetic effects on coat colour in cattle: dilution of eumelanin and phaeomelanin pigments in an F2-Backcross Charolais x Holstein population.
    Gutiérrez-Gil B, Wiener P, Williams JL.
    BMC Genet; 2007 Aug 16; 8():56. PubMed ID: 17705851
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  • 30. Linkage of the grey coat colour locus to microsatellites on horse chromosome 25.
    Locke MM, Penedo MC, Bricker SJ, Millon LV, Murray JD.
    Anim Genet; 2002 Oct 16; 33(5):329-37. PubMed ID: 12354140
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  • 31. A linkage group composed of three coat color genes and three serum protein loci in horses.
    Andersson L, Sandberg K.
    J Hered; 1982 Oct 16; 73(2):91-4. PubMed ID: 7096983
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  • 32. Novel variants in the KIT and PAX3 genes in horses with white-spotted coat colour phenotypes.
    Hauswirth R, Jude R, Haase B, Bellone RR, Archer S, Holl H, Brooks SA, Tozaki T, Penedo MC, Rieder S, Leeb T.
    Anim Genet; 2013 Dec 16; 44(6):763-5. PubMed ID: 23659293
    [Abstract] [Full Text] [Related]

  • 33. Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage interval.
    Levi A, Kohn Y, Kanyas K, Amann D, Pae CU, Hamdan A, Segman RH, Avidan N, Karni O, Korner M, Jun TY, Beckmann JS, Macciardi F, Lerer B.
    Eur J Hum Genet; 2005 Jun 16; 13(6):763-71. PubMed ID: 15812564
    [Abstract] [Full Text] [Related]

  • 34. Associations between candidate gene markers at a quantitative trait locus on equine chromosome 4 responsible for osteochondrosis dissecans in fetlock joints of South German Coldblood horses.
    Wittwer C, Dierks C, Hamann H, Distl O.
    J Hered; 2008 Jun 16; 99(2):125-9. PubMed ID: 18227080
    [Abstract] [Full Text] [Related]

  • 35. Improved resolution of the comparative horse-human map: investigating markers with in silico and linkage mapping approaches.
    Tozaki T, Swinburne J, Hirota K, Hasegawa T, Ishida N, Tobe T.
    Gene; 2007 May 01; 392(1-2):181-6. PubMed ID: 17306472
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  • 36. A novel locus for generalized epilepsy with febrile seizures plus in French families.
    Baulac S, Gourfinkel-An I, Couarch P, Depienne C, Kaminska A, Dulac O, Baulac M, LeGuern E, Nabbout R.
    Arch Neurol; 2008 Jul 01; 65(7):943-51. PubMed ID: 18625863
    [Abstract] [Full Text] [Related]

  • 37. 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 01; 152(1):29-36. PubMed ID: 15656797
    [Abstract] [Full Text] [Related]

  • 38. Isolation, characterization and chromosome assignment of 341 newly isolated equine TKY microsatellite markers.
    Tozaki T, Penedo MC, Oliveira RP, Katz JP, Millon LV, Ward T, Pettigrew DC, Brault LS, Tomita M, Kurosawa M, Hasegawa T, Hirota K.
    Anim Genet; 2004 Dec 01; 35(6):487-96. PubMed ID: 15566484
    [No Abstract] [Full Text] [Related]

  • 39. Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24.
    Schüle R, Bonin M, Dürr A, Forlani S, Sperfeld AD, Klimpe S, Mueller JC, Seibel A, van de Warrenburg BP, Bauer P, Schöls L.
    Neurology; 2009 Jun 02; 72(22):1893-8. PubMed ID: 19357379
    [Abstract] [Full Text] [Related]

  • 40. The locus for bovine dilated cardiomyopathy maps to chromosome 18.
    Guziewicz KE, Owczarek-Lipska M, Küffer J, Schelling C, Tontis A, Denis C, Eggen A, Leeb T, Dolf G, Braunschweig MH.
    Anim Genet; 2007 Jun 02; 38(3):265-9. PubMed ID: 17433012
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