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Journal Abstract Search

53 related items for PubMed ID: 8825609

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  • 3. Assignment of the human ribosomal protein S25 gene (RPS25) to chromosome 11q23.3 by sequence analysis of the marker D11S456.
    Imai T, Sudo K, Miwa T.
    Genomics; 1994 Mar 01; 20(1):142-3. PubMed ID: 8020948
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  • 4. Short report on DNA marker at candidate locus.
    Solberg K, Rødningen OK, Tonstad S, Ose L, Berg K, Leren TP.
    Clin Genet; 1993 Aug 01; 44(2):111. PubMed ID: 8275559
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  • 5. Cloning, structural characterization, and chromosomal localization of the human orthologue of Saccharomyces cerevisiae MSH5 gene.
    Her C, Doggett NA.
    Genomics; 1998 Aug 15; 52(1):50-61. PubMed ID: 9740671
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  • 8. A neocentromere derived from a supernumerary marker deleted from the long arm of chromosome 6.
    Qin N, Bartley J, Wang JC, Warburton PE.
    Cytogenet Genome Res; 2007 Aug 15; 119(1-2):154-7. PubMed ID: 18160796
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  • 10. A genome-wide scan using tree-based association analysis for candidate loci related to fasting plasma glucose levels.
    Chen CH, Chang CJ, Yang WS, Chen CL, Fann CS.
    BMC Genet; 2003 Dec 31; 4 Suppl 1(Suppl 1):S65. PubMed ID: 14975133
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  • 11. A novel gene for autosomal dominant Stargardt-like macular dystrophy with homology to the SUR4 protein family.
    Edwards AO, Donoso LA, Ritter R.
    Invest Ophthalmol Vis Sci; 2001 Oct 31; 42(11):2652-63. PubMed ID: 11581213
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  • 13. Cloning and molecular characterization of a cross-homologous zinc finger locus ZNF204.
    Partridge J, Wallace DF, Robertson A, Fox MF, Simons JP, Dooley JS, Walker AP.
    Genomics; 1998 May 15; 50(1):116-8. PubMed ID: 9628832
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  • 14. Comparative sequence analysis of the mouse and human Lgn1/SMA interval.
    Endrizzi M, Huang S, Scharf JM, Kelter AR, Wirth B, Kunkel LM, Miller W, Dietrich WF.
    Genomics; 1999 Sep 01; 60(2):137-51. PubMed ID: 10486205
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  • 15. Transcript mapping of the human chromosome 11q12-q13.1 gene-rich region identifies several newly described conserved genes.
    Cooper PR, Nowak NJ, Higgins MJ, Church DM, Shows TB.
    Genomics; 1998 May 01; 49(3):419-29. PubMed ID: 9615227
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  • 16. Testing for linkage of eye tracking dysfunction and schizophrenia to markers on chromosomes 6, 8, 9, 20, and 22 in families multiply affected with schizophrenia.
    Arolt V, Lencer R, Purmann S, Schürmann M, Müller-Myhsok B, Krecker K, Schwinger E.
    Am J Med Genet; 1999 Dec 15; 88(6):603-6. PubMed ID: 10581476
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  • 17. The relationship between chromosome structure and function at a human telomeric region.
    Flint J, Thomas K, Micklem G, Raynham H, Clark K, Doggett NA, King A, Higgs DR.
    Nat Genet; 1997 Mar 15; 15(3):252-7. PubMed ID: 9054936
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  • 18. Chromosomal mapping of the human and murine orphan receptors ERRalpha (ESRRA) and ERRbeta (ESRRB) and identification of a novel human ERRalpha-related pseudogene.
    Sladek R, Beatty B, Squire J, Copeland NG, Gilbert DJ, Jenkins NA, Giguère V.
    Genomics; 1997 Oct 15; 45(2):320-6. PubMed ID: 9344655
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  • 20. Peaks of linkage are localized by a BAC/PAC contig of the 6p reading disability locus.
    Ahn J, Won TW, Zia A, Reutter H, Kaplan DE, Sparks R, Gruen JR.
    Genomics; 2001 Nov 15; 78(1-2):19-29. PubMed ID: 11707069
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