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Journal Abstract Search

193 related items for PubMed ID: 17107390

  • 21. A genome-wide linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of Cuba.
    Marcheco-Teruel B, Flint TJ, Wikman FP, Torralbas M, González L, Blanco L, Tan Q, Ewald H, Orntoft T, Kruse TA, Børglum AD, Mors O.
    Am J Med Genet B Neuropsychiatr Genet; 2006 Dec 05; 141B(8):833-43. PubMed ID: 16917938
    [Abstract] [Full Text] [Related]

  • 22. Evidence for a novel autosomal dominant retinitis pigmentosa linked to chromosome 1p22.1-q12 in a Chinese family.
    Yuan Y, Zhou X, Wang F, Yan M, Ding F.
    Curr Eye Res; 2011 Feb 05; 36(2):154-67. PubMed ID: 21281067
    [Abstract] [Full Text] [Related]

  • 23. Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis.
    Lin MW, Lee DD, Liu TT, Lin YF, Chen SY, Huang CC, Weng HY, Liu YF, Tanaka A, Arita K, Lai-Cheong J, Palisson F, Chang YT, Wong CK, Matsuura I, McGrath JA, Tsai SF.
    Eur J Hum Genet; 2010 Jan 05; 18(1):26-32. PubMed ID: 19690585
    [Abstract] [Full Text] [Related]

  • 24. Genome-wide linkage scan for prostate cancer susceptibility genes in men with aggressive disease: significant evidence for linkage at chromosome 15q12.
    Lange EM, Ho LA, Beebe-Dimmer JL, Wang Y, Gillanders EM, Trent JM, Lange LA, Wood DP, Cooney KA.
    Hum Genet; 2006 May 05; 119(4):400-7. PubMed ID: 16508751
    [Abstract] [Full Text] [Related]

  • 25. A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder.
    DeLisi LE, Shaw SH, Crow TJ, Shields G, Smith AB, Larach VW, Wellman N, Loftus J, Nanthakumar B, Razi K, Stewart J, Comazzi M, Vita A, Heffner T, Sherrington R.
    Am J Psychiatry; 2002 May 05; 159(5):803-12. PubMed ID: 11986135
    [Abstract] [Full Text] [Related]

  • 26. A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees.
    Jasinska AJ, Service S, Jawaheer D, DeYoung J, Levinson M, Zhang Z, Kremeyer B, Muller H, Aldana I, Garcia J, Restrepo G, Lopez C, Palacio C, Duque C, Parra M, Vega J, Ortiz D, Bedoya G, Mathews C, Davanzo P, Fournier E, Bejarano J, Ramirez M, Araya Ortiz C, Araya X, Molina J, Sabatti C, Reus V, Ospina J, Macaya G, Ruiz-Linares A, Freimer NB.
    Am J Med Genet B Neuropsychiatr Genet; 2009 Oct 05; 150B(7):998-1006. PubMed ID: 19319892
    [Abstract] [Full Text] [Related]

  • 27. Genome-wide linkage scan of a large family with IgA nephropathy localizes a novel susceptibility locus to chromosome 2q36.
    Paterson AD, Liu XQ, Wang K, Magistroni R, Song X, Kappel J, Klassen J, Cattran D, St George-Hyslop P, Pei Y.
    J Am Soc Nephrol; 2007 Aug 05; 18(8):2408-15. PubMed ID: 17634434
    [Abstract] [Full Text] [Related]

  • 28. Mapping a novel locus for familial atrial fibrillation on chromosome 10p11-q21.
    Volders PG, Zhu Q, Timmermans C, Eurlings PM, Su X, Arens YH, Li L, Jongbloed RJ, Xia M, Rodriguez LM, Chen YH.
    Heart Rhythm; 2007 Apr 05; 4(4):469-75. PubMed ID: 17399636
    [Abstract] [Full Text] [Related]

  • 29. An international collaborative family-based whole-genome linkage scan for high-grade myopia.
    Li YJ, Guggenheim JA, Bulusu A, Metlapally R, Abbott D, Malecaze F, Calvas P, Rosenberg T, Paget S, Creer RC, Kirov G, Owen MJ, Zhao B, White T, Mackey DA, Young TL.
    Invest Ophthalmol Vis Sci; 2009 Jul 05; 50(7):3116-27. PubMed ID: 19324860
    [Abstract] [Full Text] [Related]

  • 30. A genome-wide search for type 2 diabetes susceptibility genes in Utah Caucasians.
    Elbein SC, Hoffman MD, Teng K, Leppert MF, Hasstedt SJ.
    Diabetes; 1999 May 05; 48(5):1175-82. PubMed ID: 10331426
    [Abstract] [Full Text] [Related]

  • 31. Genomewide scans in North American families reveal genetic linkage of essential tremor to a region on chromosome 6p23.
    Shatunov A, Sambuughin N, Jankovic J, Elble R, Lee HS, Singleton AB, Dagvadorj A, Ji J, Zhang Y, Kimonis VE, Hardy J, Hallett M, Goldfarb LG.
    Brain; 2006 Sep 05; 129(Pt 9):2318-31. PubMed ID: 16702189
    [Abstract] [Full Text] [Related]

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  • 33. Genome-wide linkage analysis reveals evidence for four new susceptibility loci for familial euthyroid goiter.
    Bayer Y, Neumann S, Meyer B, Rüschendorf F, Reske A, Brix T, Hegedüs L, Langer P, Nürnberg P, Paschke R.
    J Clin Endocrinol Metab; 2004 Aug 05; 89(8):4044-52. PubMed ID: 15292347
    [Abstract] [Full Text] [Related]

  • 34. 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 05; 14(5):492-500. PubMed ID: 18227837
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  • 36. High-density genome scan in Crohn disease shows confirmed linkage to chromosome 14q11-12.
    Duerr RH, Barmada MM, Zhang L, Pfützer R, Weeks DE.
    Am J Hum Genet; 2000 Jun 05; 66(6):1857-62. PubMed ID: 10747815
    [Abstract] [Full Text] [Related]

  • 37. A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity.
    Conte ML, Bertoli-Avella AM, de Graaf BM, Punzo F, Lama G, La Manna A, Grassia C, Rambaldi PF, Oostra BA, Perrotta S.
    Pediatr Nephrol; 2008 Apr 05; 23(4):587-95. PubMed ID: 18197425
    [Abstract] [Full Text] [Related]

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  • 39. Genome-wide linkage scan identifies a novel genetic locus on chromosome 5p13 for neonatal atrial fibrillation associated with sudden death and variable cardiomyopathy.
    Oberti C, Wang L, Li L, Dong J, Rao S, Du W, Wang Q.
    Circulation; 2004 Dec 21; 110(25):3753-9. PubMed ID: 15596564
    [Abstract] [Full Text] [Related]

  • 40. Linkage of Paget disease of bone to a novel region on human chromosome 18q23.
    Good DA, Busfield F, Fletcher BH, Duffy DL, Kesting JB, Andersen J, Shaw JT.
    Am J Hum Genet; 2002 Feb 21; 70(2):517-25. PubMed ID: 11742440
    [Abstract] [Full Text] [Related]

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