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Journal Abstract Search

266 related items for PubMed ID: 21041550

  • 1. The identification of a novel locus for mandibular prognathism in the Han Chinese population.
    Li Q, Li X, Zhang F, Chen F.
    J Dent Res; 2011 Jan; 90(1):53-7. PubMed ID: 21041550
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  • 2. Genome scan for locus involved in mandibular prognathism in pedigrees from China.
    Li Q, Zhang F, Li X, Chen F.
    PLoS One; 2010 Sep 10; 5(9):. PubMed ID: 20844756
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  • 3. Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?
    Lohmann-Hedrich K, Neumann A, Kleensang A, Lohnau T, Muhle H, Djarmati A, König IR, Pramstaller PP, Schwinger E, Kramer PL, Ziegler A, Stephani U, Klein C.
    Neurology; 2008 Feb 26; 70(9):686-94. PubMed ID: 18032746
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  • 4. Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis.
    Holliday EG, McLean DE, Nyholt DR, Mowry BJ.
    Arch Gen Psychiatry; 2009 Oct 26; 66(10):1058-67. PubMed ID: 19805696
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  • 6. 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 26; 63(11):1591-8. PubMed ID: 17101828
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  • 7. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.
    Br J Dermatol; 2005 Jan 26; 152(1):29-36. PubMed ID: 15656797
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  • 13. Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel.
    Ocaka L, Zhao C, Reed JA, Ebenezer ND, Brice G, Morley T, Mehta M, O'Dowd J, Weber JL, Hardcastle AJ, Child AH.
    J Med Genet; 2008 Feb 26; 45(2):87-92. PubMed ID: 17932119
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  • 14. Linkage analysis in keratoconus: replication of locus 5q21.2 and identification of other suggestive Loci.
    Bisceglia L, De Bonis P, Pizzicoli C, Fischetti L, Laborante A, Di Perna M, Giuliani F, Delle Noci N, Buzzonetti L, Zelante L.
    Invest Ophthalmol Vis Sci; 2009 Mar 26; 50(3):1081-6. PubMed ID: 18978346
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  • 15. Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3.
    Hedera P, Blair MA, Andermann E, Andermann F, D'Agostino D, Taylor KA, Chahine L, Pandolfo M, Bradford Y, Haines JL, Abou-Khalil B.
    Neurology; 2007 Jun 12; 68(24):2107-12. PubMed ID: 17377072
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  • 16. [A genomewide scan for the susceptibility gene loci to ankylosing spondylitis in Chinese Han population].
    Gu MM, Yuan WT, Yang JQ, Zhang J, Xiong XY, Yao FJ, Lu ZY, Wang ZG, Huang W, Fan LA.
    Yi Chuan Xue Bao; 2004 Mar 12; 31(3):217-20. PubMed ID: 15195556
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  • 17. Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family.
    de Kovel CG, Hol FA, Heister JG, Willemen JJ, Sandkuijl LA, Franke B, Padberg GW.
    J Med Genet; 2004 Sep 12; 41(9):652-7. PubMed ID: 15342694
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  • 19. 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 12; 36(8):627-33. PubMed ID: 19552635
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