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Journal Abstract Search

175 related items for PubMed ID: 14733810

  • 1. [Analysis of haplotype-based haplotype relative risk and transmission disequilibrium test in childhood absence epilepsy].
    Ge X, Wang ZP, Zhang YF, Shao XH, Bao KR.
    Zhonghua Er Ke Za Zhi; 2003 Sep; 41(9):675-9. PubMed ID: 14733810
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  • 2. Analysis of childhood absence epilepsy using haplotype-based haplotype relative risk and transmission disequilibrium test.
    Zhiping W, Xin G, Xiaoqing L, Yafen Z.
    Brain Dev; 2004 Sep; 26(6):367-72. PubMed ID: 15275697
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  • 6. Mapping and positional cloning of common idiopathic generalized epilepsies: juvenile myoclonus epilepsy and childhood absence epilepsy.
    Delgado-Escueta AV, Medina MT, Serratosa JM, Castroviejo IP, Gee MN, Weissbecker K, Westling BW, Fong CY, Alonso ME, Cordova S, Shah P, Khan S, Sainz J, Rubio-Donnadieu F, Sparkes RS.
    Adv Neurol; 1999 Sep; 79():351-74. PubMed ID: 10514826
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  • 8. [Transmission disequilibrium analysis of 1137-1140 Del GTGA frameshift mutation within the KCNN3 gene and schizophrenia based on family trios].
    Hong XH, Xu CT, Yang Q, Wu CR.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):441-3. PubMed ID: 16086287
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  • 9. Common polymorphisms in the CACNA1H gene associated with childhood absence epilepsy in Chinese Han population.
    Liang J, Zhang Y, Chen Y, Wang J, Pan H, Wu H, Xu K, Liu X, Jiang Y, Shen Y, Wu X.
    Ann Hum Genet; 2007 May; 71(Pt 3):325-35. PubMed ID: 17156077
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  • 10. Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q.
    Robinson R, Taske N, Sander T, Heils A, Whitehouse W, Goutières F, Aicardi J, Lehesjoki AE, Siren A, Laue Friis M, Kjeldsen MJ, Panayiotopoulos C, Kennedy C, Ferrie C, Rees M, Gardiner RM.
    Epilepsy Res; 2002 Feb; 48(3):169-79. PubMed ID: 11904235
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  • 13. Family-based association study of Tim-1 and Tim-3 gene polymorphisms with childhood asthma in Chinese trios.
    Wu QW, Cai PC, Wang L, Li YR, Kong LL, Hu LH.
    Int Arch Allergy Immunol; 2009 Feb; 150(3):252-60. PubMed ID: 19494522
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  • 14. Role of Fcgamma receptors IIA, IIIA, and IIIB in susceptibility to rheumatoid arthritis.
    Radstake TR, Petit E, Pierlot C, van de Putte LB, Cornelis F, Barrera P.
    J Rheumatol; 2003 May; 30(5):926-33. PubMed ID: 12734884
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  • 18. T-STAR gene: fine mapping in the candidate region for childhood absence epilepsy on 8q24 and mutational analysis in patients.
    Sugimoto Y, Morita R, Amano K, Shah PU, Pascual-Castroviejo I, Khan S, Delgado-Escueta AV, Yamakawa K.
    Epilepsy Res; 2001 Aug; 46(2):139-44. PubMed ID: 11463515
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