Search Results - Smit, L.M.E.

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  1. 1
    Bilateral foot drop as the first symptom of nemaline myopathy

    Bilateral foot drop as the first symptom of nemaline myopathy by Hoeksema, D.G., Linssen, W.H.J.P., Smit, L.M.E.

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  2. 2
    Two sisters with autosomal recessive limb-girdle muscular dystrophy with gamma-sarcoglycanopathy (LGMD2C)

    Two sisters with autosomal recessive limb-girdle muscular dystrophy with gamma-sarcoglycanopathy (LGMD2C) by Broere, D., Linssen, W.H.J.P., Smit, L.M.E., Ginjaar, H.B.

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    Two sisters with sever childhood recessive muscular dystrophy (SCARMD) with a γ-sarcoglycanopathy maped on chromosome 13q12

    Two sisters with sever childhood recessive muscular dystrophy (SCARMD) with a γ-sarcoglycanopathy maped on chromosome 13q12 by Broere, D., Linssen, W.H.J.P., Ginjaar, H.B., Smit, L.M.E.

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  4. 4
    316 A Dutch pedigree with a deletion in the muscle promoter region of dystrophin presenting with various phenotypes

    316 A Dutch pedigree with a deletion in the muscle promoter region of dystrophin presenting with various phenotypes by Broere, D., Smit, L.M.E., Ginjaar, H.B., Visscher, F., Drexhage, V.E., De Visser, M.

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