G.O.4 von van den Boogaard, T.L, Lemmers, R.J.L, Camano, P, van der Vliet, P.J, Balog, J, Voermans, N, Tapscott, S.J, de Munain, A.L, Tawil, R, Bakker, B, Maarel, S.M

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O.19 Facioscapulohumeral muscular dystrophy: Muscle running out of control von Lemmers, R.J.L, van der Vliet, P.J, Sacconi, S, Camano, P, Snider, L, Geng, L, van Ommen, G.J, Padberg, G.W, Miller, D.G, Tapscott, S.J, Frants, R.R, van der Maarel, S.M

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G.O.4: The SMCHD1 mutation spectrum in FSHD2: Novel insight in clinical variability in FSHD von van den Boogaard, T.L., Lemmers, R.J.L., Camano, P., van der Vliet, P.J., Balog, J., Voermans, N., Tapscott, S.J., de Munain, A.L., Tawil, R., Bakker, B., Maarel, S.M.

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G.O.3 Contraction-dependent (FSHD1) and independent (FSHD2) epigenetic changes of D4Z4 unify FSHD von de Greef, J.C., Lemmers, R.J.L., van Engelen, B.G.M., Sacconi, S., Venance, S.L., Frants, R.R., Tawil, R., van der Maarel, S.M.

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G.O.3 Contraction-dependent (FSHD1) and independent (FSHD2) epigenetic changes of D4Z4 unify FSHD von de Greef, J.C, Lemmers, R.J.L, van Engelen, B.G.M, Sacconi, S, Venance, S.L, Frants, R.R, Tawil, R, van der Maarel, S.M

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