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Journal Abstract Search

305 related items for PubMed ID: 16084785

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  • 3. Genome-wide scan of African-American and white families for linkage to myopia.
    Ciner E, Ibay G, Wojciechowski R, Dana D, Holmes TN, Bailey-Wilson JE, Stambolian D.
    Am J Ophthalmol; 2009 Mar; 147(3):512-517.e2. PubMed ID: 19026404
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  • 4. A chromosome 14 risk locus for simple phobia: results from a genomewide linkage scan.
    Gelernter J, Page GP, Bonvicini K, Woods SW, Pauls DL, Kruger S.
    Mol Psychiatry; 2003 Jan; 8(1):71-82. PubMed ID: 12556910
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  • 5. Identification of a novel locus on 2q for autosomal dominant high-grade myopia.
    Paluru PC, Nallasamy S, Devoto M, Rappaport EF, Young TL.
    Invest Ophthalmol Vis Sci; 2005 Jul; 46(7):2300-7. PubMed ID: 15980214
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  • 6. Genetic linkage mapping for a susceptibility locus to bipolar illness: chromosomes 2, 3, 4, 7, 9, 10p, 11p, 22, and Xpter.
    Detera-Wadleigh SD, Hsieh WT, Berrettini WH, Goldin LR, Rollins DY, Muniec D, Grewal R, Guroff JJ, Turner G, Coffman D.
    Am J Med Genet; 1994 Sep 15; 54(3):206-18. PubMed ID: 7810578
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  • 7. Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24.
    Lerer B, Segman RH, Hamdan A, Kanyas K, Karni O, Kohn Y, Korner M, Lanktree M, Kaadan M, Turetsky N, Yakir A, Kerem B, Macciardi F.
    Mol Psychiatry; 2003 May 15; 8(5):488-98. PubMed ID: 12808429
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  • 8. Results of a genome-wide linkage analysis in prostate cancer families ascertained through the ACTANE consortium.
    Edwards S, Meitz J, Eles R, Evans C, Easton D, Hopper J, Giles G, Foulkes WD, Narod S, Simard J, Badzioch M, Mahle L, International ACTANE Consortium.
    Prostate; 2003 Dec 01; 57(4):270-9. PubMed ID: 14601023
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  • 9. Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands.
    Hanna GL, Veenstra-VanderWeele J, Cox NJ, Boehnke M, Himle JA, Curtis GC, Leventhal BL, Cook EH.
    Am J Med Genet; 2002 Jul 08; 114(5):541-52. PubMed ID: 12116192
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  • 10. Genome-wide linkage analysis of 160 North American families with celiac disease.
    Garner CP, Ding YC, Steele L, Book L, Leiferman K, Zone JJ, Neuhausen SL.
    Genes Immun; 2007 Mar 08; 8(2):108-14. PubMed ID: 17136122
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  • 11. Clinical description and genome wide linkage study of Y-sutural cataract and myopia in a Chinese family.
    Zhang Q, Guo X, Xiao X, Yi J, Jia X, Hejtmancik JF.
    Mol Vis; 2004 Nov 17; 10():890-900. PubMed ID: 15570218
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  • 12. Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease.
    Lee JH, Cheng R, Santana V, Williamson J, Lantigua R, Medrano M, Arriaga A, Stern Y, Tycko B, Rogaeva E, Wakutani Y, Kawarai T, St George-Hyslop P, Mayeux R.
    Arch Neurol; 2006 Nov 17; 63(11):1591-8. PubMed ID: 17101828
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  • 13. Genome-wide linkage analysis for celiac disease in North American families.
    Neuhausen SL, Feolo M, Camp NJ, Farnham J, Book L, Zone JJ.
    Am J Med Genet; 2002 Jul 22; 111(1):1-9. PubMed ID: 12124726
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  • 14. A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19.
    Badenhop RF, Moses MJ, Scimone A, Mitchell PB, Ewen-White KR, Rosso A, Donald JA, Adams LJ, Schofield PR.
    Mol Psychiatry; 2002 Jul 22; 7(6):594-603. PubMed ID: 12140782
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  • 16. [The human major histocompatibility complex region is not a major susceptibility locus for Graves disease among the Hans in north of China].
    Jin Y, Hu F, Teng W, Ben S, Zhang J, Xiong X, Huang W.
    Zhonghua Yi Xue Za Zhi; 2002 Sep 25; 82(18):1242-4. PubMed ID: 12425802
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  • 18. Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scan.
    Kemp Z, Carvajal-Carmona L, Spain S, Barclay E, Gorman M, Martin L, Jaeger E, Brooks N, Bishop DT, Thomas H, Tomlinson I, Papaemmanuil E, Webb E, Sellick GS, Wood W, Evans G, Lucassen A, Maher ER, Houlston RS, ColoRectal tumour Gene Identification (CoRGI) Study Consortium.
    Hum Mol Genet; 2006 Oct 01; 15(19):2903-10. PubMed ID: 16923799
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  • 19. Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects.
    Loo SK, Fisher SE, Francks C, Ogdie MN, MacPhie IL, Yang M, McCracken JT, McGough JJ, Nelson SF, Monaco AP, Smalley SL.
    Mol Psychiatry; 2004 May 01; 9(5):485-93. PubMed ID: 14625563
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  • 20. Further evidence of genetic heterogeneity segregating with hereditary gingival fibromatosis.
    Ye X, Shi L, Yin W, Meng L, Wang QK, Bian Z.
    J Clin Periodontol; 2009 Aug 01; 36(8):627-33. PubMed ID: 19552635
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