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Pubmed for Handhelds

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Journal Abstract Search

448 related items for PubMed ID: 17435464

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  • 4. Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways.
    Nishimura Y, Martin CL, Vazquez-Lopez A, Spence SJ, Alvarez-Retuerto AI, Sigman M, Steindler C, Pellegrini S, Schanen NC, Warren ST, Geschwind DH.
    Hum Mol Genet; 2007 Jul 15; 16(14):1682-98. PubMed ID: 17519220
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  • 7. Molecular markers for diagnosis of Prader-Willi syndrome in thai patients by fish.
    Wiriyaukaradecha S, Patmasiriwat P, Wasant P, Tantiniti P.
    Southeast Asian J Trop Med Public Health; 2003 Dec 15; 34(4):881-6. PubMed ID: 15115105
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  • 8. Neonatal diagnosis of Prader-Willi syndrome and its implications.
    Greenberg F, Elder FF, Ledbetter DH.
    Am J Med Genet; 1987 Dec 15; 28(4):845-56. PubMed ID: 3688023
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  • 11. Elimination disorders in persons with Prader-Willi and Fragile-X syndromes.
    Equit M, Piro-Hussong A, Niemczyk J, Curfs L, von Gontard A.
    Neurourol Urodyn; 2013 Sep 15; 32(7):986-92. PubMed ID: 23239431
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  • 14. Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.
    Gilhuis HJ, van Ravenswaaij CM, Hamel BJ, Gabreëls FJ.
    Eur J Paediatr Neurol; 2000 Sep 15; 4(1):39-43. PubMed ID: 10701104
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  • 15. Altered expression of Autism-associated genes in the brain of Fragile X mouse model.
    Zhang A, Shen CH, Ma SY, Ke Y, El Idrissi A.
    Biochem Biophys Res Commun; 2009 Feb 20; 379(4):920-3. PubMed ID: 19138667
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  • 16. [Prader-Willi syndrome in 22-year-old man--case study].
    Kardas P, Adamiak-Kardas M.
    Wiad Lek; 2001 Feb 20; 54(11-12):709-14. PubMed ID: 11928560
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  • 17. Molecular diagnosis of Prader-Willi syndrome.
    Pangkanon S.
    J Med Assoc Thai; 2003 Aug 20; 86 Suppl 3():S510-6. PubMed ID: 14700141
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  • 18. The fragile X syndrome: exploring its molecular basis and seeking a treatment.
    Bardoni B, Davidovic L, Bensaid M, Khandjian EW.
    Expert Rev Mol Med; 2006 Apr 21; 8(8):1-16. PubMed ID: 16626504
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  • 19. Social behavior phenotypes in fragile X syndrome, autism, and the Fmr1 knockout mouse: theoretical comment on McNaughton et al. (2008).
    Brodkin ES.
    Behav Neurosci; 2008 Apr 21; 122(2):483-9. PubMed ID: 18410188
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