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PUBMED FOR HANDHELDS

Journal Abstract Search


106 related items for PubMed ID: 6214946

  • 21. [Spina bifida: an equivalent mutation in man of the mouse T locus?].
    Fellous M.
    Presse Med; 1985 Jan 26; 14(3):135-6. PubMed ID: 3156335
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  • 23. Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping.
    Nürnberg G, Jacobi FK, Broghammer M, Becker C, Blin N, Nürnberg P, Stephani U, Pusch CM.
    Int J Mol Med; 2008 Apr 26; 21(4):429-38. PubMed ID: 18360688
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  • 29. HLA gene and haplotype frequencies in spina bifida. Population and family studies.
    De Bruyere M, Kulakowski S, Malchaire J, Delire M, Sokal G.
    Tissue Antigens; 1977 Nov 26; 10(5):399-402. PubMed ID: 605436
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  • 31. Prevalence of sacral spina bifida occulta and its relationship to age, sex, race, and the sacral table angle: an anatomic, osteologic study of three thousand one hundred specimens.
    Eubanks JD, Cheruvu VK.
    Spine (Phila Pa 1976); 2009 Jul 01; 34(15):1539-43. PubMed ID: 19564762
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  • 32. Spina bifida occulta. Incidence in parents of offspring with spina bifida cystica.
    Schweitzer ME, Balsam D, Weiss R.
    Spine (Phila Pa 1976); 1993 May 01; 18(6):785-6. PubMed ID: 8516715
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  • 33. Linkage analyses of chromosome 6 loci, including HLA, in familial aggregations of Crohn disease. G.E.T.A.I.D.
    Hugot JP, Laurent-Puig P, Gower-Rousseau C, Caillat-Zucman S, Beaugerie L, Dupas JL, Van Gossum A, Bonäit-Pellie C, Cortot A, Thomas G.
    Am J Med Genet; 1994 Aug 15; 52(2):207-13. PubMed ID: 7802010
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  • 36. Constipation is associated with spina bifida occulta in children.
    Yuan Z, Cheng W, Hou A, Wang W, Zhang S, Liu D, Gao F, Li H, Wang W.
    Clin Gastroenterol Hepatol; 2008 Dec 15; 6(12):1348-53. PubMed ID: 19081525
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  • 37. Contribution to the etiology of spina bifida cystica.
    Sulla I, Fagula J, Magdo J, Vasko G, Vyrostko J.
    Zentralbl Neurochir; 1984 Dec 15; 45(3):179-82. PubMed ID: 6391039
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  • 38. Identification of a novel locus for febrile seizures and epilepsy on chromosome 21q22.
    Hedera P, Ma S, Blair MA, Taylor KA, Hamati A, Bradford Y, Abou-Khalil B, Haines JL.
    Epilepsia; 2006 Oct 15; 47(10):1622-8. PubMed ID: 17054683
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  • 39. A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3.
    Straub RE, Lehner T, Luo Y, Loth JE, Shao W, Sharpe L, Alexander JR, Das K, Simon R, Fieve RR.
    Nat Genet; 1994 Nov 15; 8(3):291-6. PubMed ID: 7874172
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  • 40. Sacral agenesis occurring in siblings: case report.
    Muthukumar N, Gurunathan J, Sampathkumar M, Gajendran R.
    Neurosurgery; 1992 Jun 15; 30(6):946-8. PubMed ID: 1614603
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