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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

298 related items for PubMed ID: 25545674

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  • 27. Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2.
    Calandra P, Cascino I, Lemmers RJ, Galluzzi G, Teveroni E, Monforte M, Tasca G, Ricci E, Moretti F, van der Maarel SM, Deidda G.
    J Med Genet; 2016 May; 53(5):348-55. PubMed ID: 26831754
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  • 34. Nanopore-based single molecule sequencing of the D4Z4 array responsible for facioscapulohumeral muscular dystrophy.
    Mitsuhashi S, Nakagawa S, Takahashi Ueda M, Imanishi T, Frith MC, Mitsuhashi H.
    Sci Rep; 2017 Nov 01; 7(1):14789. PubMed ID: 29093467
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  • 36. Molecular basis of facioscapulohumeral muscular dystrophy.
    Tupler R, Gabellini D.
    Cell Mol Life Sci; 2004 Mar 01; 61(5):557-566. PubMed ID: 15004695
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  • 37. Polycomb repressive complex 1 provides a molecular explanation for repeat copy number dependency in FSHD muscular dystrophy.
    Casa V, Runfola V, Micheloni S, Aziz A, Dilworth FJ, Gabellini D.
    Hum Mol Genet; 2017 Feb 15; 26(4):753-767. PubMed ID: 28040729
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