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Journal Abstract Search

173 related items for PubMed ID: 10889536

  • 21. A discordant sib-pair linkage analysis of age-related macular degeneration.
    Santangelo SL, Yen CH, Haddad S, Fagerness J, Huang C, Seddon JM.
    Ophthalmic Genet; 2005 Jun; 26(2):61-7. PubMed ID: 16020308
    [Abstract] [Full Text] [Related]

  • 22. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
    Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA.
    Mol Psychiatry; 2007 Apr; 12(4):376-84. PubMed ID: 17179998
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  • 23. An autosomal genomic screen for autism.
    Collaborative Linkage Study of Autism.
    Am J Med Genet; 2001 Dec 08; 105(8):609-15. PubMed ID: 11811142
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  • 24. Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16.
    Wassink TH, Vieland VJ, Sheffield VC, Bartlett CW, Goedken R, Childress D, Piven J.
    Psychiatr Genet; 2008 Apr 08; 18(2):85-91. PubMed ID: 18349700
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  • 25. [Genetics of autism: from genome scans to candidate genes].
    Jamain S, Betancur C, Giros B, Leboyer M, Bourgeron T.
    Med Sci (Paris); 2003 Nov 08; 19(11):1081-90. PubMed ID: 14648479
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  • 27. Incorporating language phenotypes strengthens evidence of linkage to autism.
    Bradford Y, Haines J, Hutcheson H, Gardiner M, Braun T, Sheffield V, Cassavant T, Huang W, Wang K, Vieland V, Folstein S, Santangelo S, Piven J.
    Am J Med Genet; 2001 Aug 08; 105(6):539-47. PubMed ID: 11496372
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  • 28. Incorporating language phenotypes strengthens evidence of linkage to autism.
    Collaborative Linkage Study of Autism.
    Am J Med Genet; 2001 Dec 08; 105(8):539-47. PubMed ID: 11811141
    [Abstract] [Full Text] [Related]

  • 29. High-density mapping and follow-up studies on chromosomal regions 1, 3, 6, 12, 13 and 17 in 28 families with chronic lymphocytic leukaemia.
    Ng D, Marti GE, Fontaine L, Toro JR, Caporaso N, Goldin LR.
    Br J Haematol; 2006 Apr 08; 133(1):59-61. PubMed ID: 16512829
    [Abstract] [Full Text] [Related]

  • 30. A genomic screen of autism: evidence for a multilocus etiology.
    Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, Hallmayer J, Kalaydjieva L, McCague P, Dimiceli S, Pitts T, Nguyen L, Yang J, Harper C, Thorpe D, Vermeer S, Young H, Hebert J, Lin A, Ferguson J, Chiotti C, Wiese-Slater S, Rogers T, Salmon B, Nicholas P, Petersen PB, Pingree C, McMahon W, Wong DL, Cavalli-Sforza LL, Kraemer HC, Myers RM.
    Am J Hum Genet; 1999 Aug 08; 65(2):493-507. PubMed ID: 10417292
    [Abstract] [Full Text] [Related]

  • 31. Identification of Chromosomal Regions Linked to Diabetic Nephropathy: A Meta-Analysis of Genome-Wide Linkage Scans.
    Tziastoudi M, Stefanidis I, Stravodimos K, Zintzaras E.
    Genet Test Mol Biomarkers; 2019 Feb 08; 23(2):105-117. PubMed ID: 30694714
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  • 33. Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36.
    Field LL, Shumansky K, Ryan J, Truong D, Swiergala E, Kaplan BJ.
    Genes Brain Behav; 2013 Feb 08; 12(1):56-69. PubMed ID: 23190410
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  • 36. Evidence for multiple loci from a genome scan of autism kindreds.
    Schellenberg GD, Dawson G, Sung YJ, Estes A, Munson J, Rosenthal E, Rothstein J, Flodman P, Smith M, Coon H, Leong L, Yu CE, Stodgell C, Rodier PM, Spence MA, Minshew N, McMahon WM, Wijsman EM.
    Mol Psychiatry; 2006 Nov 08; 11(11):1049-60, 979. PubMed ID: 16880825
    [Abstract] [Full Text] [Related]

  • 37. Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16.
    Chapman NH, Estes A, Munson J, Bernier R, Webb SJ, Rothstein JH, Minshew NJ, Dawson G, Schellenberg GD, Wijsman EM.
    Hum Genet; 2011 Jan 08; 129(1):59-70. PubMed ID: 20963441
    [Abstract] [Full Text] [Related]

  • 38. Type 1 diabetes: evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families.
    Concannon P, Erlich HA, Julier C, Morahan G, Nerup J, Pociot F, Todd JA, Rich SS, Type 1 Diabetes Genetics Consortium.
    Diabetes; 2005 Oct 08; 54(10):2995-3001. PubMed ID: 16186404
    [Abstract] [Full Text] [Related]

  • 39. Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland.
    Auranen M, Varilo T, Alen R, Vanhala R, Ayers K, Kempas E, Ylisaukko-Oja T, Peltonen L, Järvelä I.
    Mol Psychiatry; 2003 Oct 08; 8(10):879-84. PubMed ID: 14515138
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  • 40. Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 4, 7, 9, 18, 19, 20, and 21q.
    Detera-Wadleigh SD, Badner JA, Yoshikawa T, Sanders AR, Goldin LR, Turner G, Rollins DY, Moses T, Guroff JJ, Kazuba D, Maxwell ME, Edenberg HJ, Foroud T, Lahiri D, Nurnberger JI, Stine OC, McMahon F, Meyers DA, MacKinnon D, Simpson S, McInnis M, DePaulo JR, Rice J, Goate A, Gershon ES.
    Am J Med Genet; 1997 May 31; 74(3):254-62. PubMed ID: 9184307
    [Abstract] [Full Text] [Related]

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