Works matching DE "MUSCLE dysmorphia"

Results: 372
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    Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation.

    Published in:
    PLoS Genetics, 2019, v. 15, n. 2, p. 1, doi. 10.1371/journal.pgen.1007917
    By:
    • O’Connell, Amy E.;
    • Gerashchenko, Maxim V.;
    • O’Donohue, Marie-Francoise;
    • Rosen, Samantha M.;
    • Huntzinger, Eric;
    • Gleeson, Diane;
    • Galli, Antonella;
    • Ryder, Edward;
    • Cao, Siqi;
    • Murphy, Quinn;
    • Kazerounian, Shideh;
    • Morton, Sarah U.;
    • Schmitz-Abe, Klaus;
    • Gladyshev, Vadim N.;
    • Gleizes, Pierre-Emmanuel;
    • Séraphin, Bertrand;
    • Agrawal, Pankaj B.
    Publication type:
    Article
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    Diastematomyelia - Imaging Findings, Case Report.

    Published in:
    Current Health Sciences Journal, 2016, v. 42, n. 1, p. 94, doi. 10.12865/CHSJ.42.01.13
    By:
    • ALBULESCU, DANA;
    • ALBU, CARMEN;
    • CONSTANTIN, C.;
    • STOICA, ZOIA;
    • NICOLESCU, IULIANA
    Publication type:
    Article
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    The Twiddling Andersen.

    Published in:
    2009
    By:
    • Jefferies, John L.;
    • Kim, Jeffrey J.;
    • Belmont, John W.;
    • Friedman, Richard A.
    Publication type:
    Case Study
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