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Journal Abstract Search

200 related items for PubMed ID: 17408830

  • 21.
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  • 22. Association analysis of the NrCAM gene in autism and in subsets of families with severe obsessive-compulsive or self-stimulatory behaviors.
    Sakurai T, Ramoz N, Reichert JG, Corwin TE, Kryzak L, Smith CJ, Silverman JM, Hollander E, Buxbaum JD.
    Psychiatr Genet; 2006 Dec; 16(6):251-7. PubMed ID: 17106428
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  • 25. Is autism caused by early hyperactivity of brain-derived neurotrophic factor?
    Tsai SJ.
    Med Hypotheses; 2005 Dec; 65(1):79-82. PubMed ID: 15893122
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  • 28. Study of HOXD genes in autism particularly regarding the ratio of second to fourth digit length.
    Sugie Y, Sugie H, Fukuda T, Osawa J.
    Brain Dev; 2010 May; 32(5):356-61. PubMed ID: 19540081
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  • 29. Family- and population-based association studies of monoamine oxidase A and autism spectrum disorders in Korean.
    Yoo HJ, Lee SK, Park M, Cho IH, Hyun SH, Lee JC, Yang SY, Kim SA.
    Neurosci Res; 2009 Mar; 63(3):172-6. PubMed ID: 19100789
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  • 30. Promoter polymorphism in the MS4A2 gene and asthma in the Indian population.
    Sharma S, Ghosh B.
    Int Arch Allergy Immunol; 2009 Mar; 149(3):208-18. PubMed ID: 19218813
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  • 31. Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism.
    Philippi A, Roschmann E, Tores F, Lindenbaum P, Benajou A, Germain-Leclerc L, Marcaillou C, Fontaine K, Vanpeene M, Roy S, Maillard S, Decaulne V, Saraiva JP, Brooks P, Rousseau F, Hager J.
    Mol Psychiatry; 2005 Oct; 10(10):950-60. PubMed ID: 16027742
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  • 32.
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  • 33. Protein kinase C-beta 1 gene variants are not associated with autism in the Irish population.
    Yang MS, Cochrane L, Conroy J, Hawi Z, Fitzgerald M, Gallagher L, Gill M.
    Psychiatr Genet; 2007 Feb; 17(1):39-41. PubMed ID: 17167344
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  • 37. Association of the DAO and DAOA gene polymorphisms with autism spectrum disorders in boys in Korea: a preliminary study.
    Chung S, Hong JP, Yoo HK.
    Psychiatry Res; 2007 Oct 31; 153(2):179-82. PubMed ID: 17629951
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  • 39. Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions.
    Campbell DB, Buie TM, Winter H, Bauman M, Sutcliffe JS, Perrin JM, Levitt P.
    Pediatrics; 2009 Mar 31; 123(3):1018-24. PubMed ID: 19255034
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  • 40. Aberrations in folate metabolic pathway and altered susceptibility to autism.
    Mohammad NS, Jain JM, Chintakindi KP, Singh RP, Naik U, Akella RR.
    Psychiatr Genet; 2009 Aug 31; 19(4):171-6. PubMed ID: 19440165
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