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Journal Abstract Search

139 related items for PubMed ID: 16741942

  • 1. A Meniere's disease gene linked to chromosome 12p12.3.
    Klar J, Frykholm C, Friberg U, Dahl N.
    Am J Med Genet B Neuropsychiatr Genet; 2006 Jul 05; 141B(5):463-7. PubMed ID: 16741942
    [Abstract] [Full Text] [Related]

  • 2. Familiar Meniere's disease restricted to 1.48 Mb on chromosome 12p12.3 by allelic and haplotype association.
    Gabriková D, Frykholm C, Friberg U, Lahsaee S, Entesarian M, Dahl N, Klar J.
    J Hum Genet; 2010 Dec 05; 55(12):834-7. PubMed ID: 20927121
    [Abstract] [Full Text] [Related]

  • 3. High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene.
    Fransen E, Verstreken M, Verhagen WI, Wuyts FL, Huygen PL, D'Haese P, Robertson NG, Morton CC, McGuirt WT, Smith RJ, Declau F, Van de Heyning PH, Van Camp G.
    Hum Mol Genet; 1999 Aug 05; 8(8):1425-9. PubMed ID: 10400989
    [Abstract] [Full Text] [Related]

  • 4. Genetic aspects of familial Ménière's disease.
    Arweiler-Harbeck D, Horsthemke B, Jahnke K, Hennies HC.
    Otol Neurotol; 2011 Jun 05; 32(4):695-700. PubMed ID: 21436747
    [Abstract] [Full Text] [Related]

  • 5. Familial Ménière's disease in five generations.
    Frykholm C, Larsen HC, Dahl N, Klar J, Rask-Andersen H, Friberg U.
    Otol Neurotol; 2006 Aug 05; 27(5):681-6. PubMed ID: 16868516
    [Abstract] [Full Text] [Related]

  • 6. Identification of novel suggestive loci for high-grade myopia in Polish families.
    Rydzanicz M, Nath SK, Sun C, Podfigurna-Musielak M, Frajdenberg A, Mrugacz M, Winters D, Ratnamala U, Radhakrishna U, Bejjani BA, Gajecka M.
    Mol Vis; 2011 Aug 05; 17():2028-39. PubMed ID: 21850178
    [Abstract] [Full Text] [Related]

  • 7. Finnish familial Meniere disease is not linked to chromosome 12p12.3, and anticipation and cosegregation with migraine are not common findings.
    Hietikko E, Kotimäki J, Kentala E, Klockars T, Sorri M, Männikkö M.
    Genet Med; 2011 May 05; 13(5):415-20. PubMed ID: 21346584
    [Abstract] [Full Text] [Related]

  • 8. Genetic architecture of Meniere's disease.
    Gallego-Martinez A, Lopez-Escamez JA.
    Hear Res; 2020 Nov 05; 397():107872. PubMed ID: 31874721
    [Abstract] [Full Text] [Related]

  • 9. Genome-wide linkage scan for genes influencing plasma triglyceride levels in the Veterans Administration Genetic Epidemiology Study.
    Coletta DK, Schneider J, Hu SL, Dyer TD, Puppala S, Farook VS, Arya R, Lehman DM, Blangero J, DeFronzo RA, Duggirala R, Jenkinson CP.
    Diabetes; 2009 Jan 05; 58(1):279-84. PubMed ID: 18931038
    [Abstract] [Full Text] [Related]

  • 10. Homozygosity mapping of lethal congenital contractural syndrome type 2 (LCCS2) to a 6 cM interval on chromosome 12q13.
    Narkis G, Landau D, Manor E, Elbedour K, Tzemach A, Fishelson M, Geiger D, Ofir R, Carmi R, Birk OS.
    Am J Med Genet A; 2004 Oct 15; 130A(3):272-6. PubMed ID: 15378541
    [Abstract] [Full Text] [Related]

  • 11. Limbic System Associated Membrane Protein Mutation in an Iranian Family Diagnosed with Ménière's Disease.
    Mehrjoo Z, Kahrizi K, Mohseni M, Akbari M, Arzhangi S, Jalalvand K, Najmabadi H, Farhadi M, Mohseni M, Asghari A, Mohebbi S, Daneshi A.
    Arch Iran Med; 2020 May 01; 23(5):319-325. PubMed ID: 32383616
    [Abstract] [Full Text] [Related]

  • 12. Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12.
    Flex E, Mangino M, Mazzoli M, Martini A, Migliosi V, Colosimo A, Mingarelli R, Pizzuti A, Dallapiccola B.
    J Med Genet; 2003 Apr 01; 40(4):278-81. PubMed ID: 12676899
    [Abstract] [Full Text] [Related]

  • 13. Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families.
    Wong FK, Hagberg C, Karsten A, Larson O, Gustavsson M, Huggare J, Larsson C, Teh BT, Linder-Aronson S.
    Cleft Palate Craniofac J; 2000 Jul 01; 37(4):357-62. PubMed ID: 10912714
    [Abstract] [Full Text] [Related]

  • 14. A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1.
    Funayama M, Hasegawa K, Kowa H, Saito M, Tsuji S, Obata F.
    Ann Neurol; 2002 Mar 01; 51(3):296-301. PubMed ID: 11891824
    [Abstract] [Full Text] [Related]

  • 15. Localization of the gene causing keratolytic winter erythema to chromosome 8p22-p23, and evidence for a founder effect in South African Afrikaans-speakers.
    Starfield M, Hennies HC, Jung M, Jenkins T, Wienker T, Hull P, Spurdle A, Küster W, Ramsay M, Reis A.
    Am J Hum Genet; 1997 Aug 01; 61(2):370-8. PubMed ID: 9311742
    [Abstract] [Full Text] [Related]

  • 16. Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q.
    Desautels A, Turecki G, Montplaisir J, Sequeira A, Verner A, Rouleau GA.
    Am J Hum Genet; 2001 Dec 01; 69(6):1266-70. PubMed ID: 11704926
    [Abstract] [Full Text] [Related]

  • 17. Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease.
    Cabrera S, Sanchez E, Requena T, Martinez-Bueno M, Benitez J, Perez N, Trinidad G, Soto-Varela A, Santos-Perez S, Martin-Sanz E, Fraile J, Perez P, Alarcon-Riquelme ME, Batuecas A, Espinosa-Sanchez JM, Aran I, Lopez-Escamez JA.
    PLoS One; 2014 Dec 01; 9(11):e112171. PubMed ID: 25397881
    [Abstract] [Full Text] [Related]

  • 18. A new locus for inherited nuclear cataract mapped to the long arm of chromosome 1.
    Wang L, Lin H, Shen Y, Huang S, Gu J, Su H, Qi Y.
    Mol Vis; 2007 Aug 01; 13():1357-62. PubMed ID: 17768382
    [Abstract] [Full Text] [Related]

  • 19. Fine mapping of 10q and 18q for familial Alzheimer's disease in Caribbean Hispanics.
    Lee JH, Mayeux R, Mayo D, Mo J, Santana V, Williamson J, Flaquer A, Ciappa A, Rondon H, Estevez P, Lantigua R, Kawarai T, Toulina A, Medrano M, Torres M, Stern Y, Tycko B, Rogaeva E, St George-Hyslop P, Knowles JA.
    Mol Psychiatry; 2004 Nov 01; 9(11):1042-51. PubMed ID: 15241431
    [Abstract] [Full Text] [Related]

  • 20. 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]

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