Found: 3

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  • A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3.

    Published in:
    Journal of Neurodevelopmental Disorders, 2011, v. 3, n. 2, p. 124, doi. 10.1007/s11689-011-9076-5
    By:
    • Pagnamenta, Alistair;
    • Holt, Richard;
    • Yusuf, Mohammed;
    • Pinto, Dalila;
    • Wing, Kirsty;
    • Betancur, Catalina;
    • Scherer, Stephen;
    • Volpi, Emanuela;
    • Monaco, Anthony
    Publication type:
    Article

  • A 15q13.3 microdeletion segregating with autism.

    Published in:
    European Journal of Human Genetics, 2009, v. 17, n. 5, p. 687, doi. 10.1038/ejhg.2008.228
    By:
    • Pagnamenta, Alistair T.;
    • Wing, Kirsty;
    • Akha, Elham Sadighi;
    • Knight, Samantha J. L.;
    • Bölte, Sven;
    • Schmötzer, Gabriele;
    • Duketis, Eftichia;
    • Poustka, Fritz;
    • Klauck, Sabine M.;
    • Poustka, Annemarie;
    • Ragoussis, Jiannis;
    • Bailey, Anthony J.;
    • Monaco, Anthony P.
    Publication type:
    Article

  • International consensus definition of low anterior resection syndrome.

    Published in:
    ANZ Journal of Surgery, 2020, v. 90, n. 3, p. 300, doi. 10.1111/ans.15421
    By:
    • Keane, Celia;
    • Fearnhead, Nicola S.;
    • Bordeianou, Liliana G.;
    • Christensen, Peter;
    • Espin Basany, Eloy;
    • Laurberg, Søren;
    • Mellgren, Anders;
    • Messick, Craig;
    • Orangio, Guy R.;
    • Verjee, Azmina;
    • Wing, Kirsty;
    • Bissett, Ian P.
    Publication type:
    Article