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Tupler, Rossella

One or more keywords matched the following items that are connected to Tupler, Rossella

Item Type	Name
Academic Article	Facioscapulohumeral muscular dystrophy: new insights from compound heterozygotes and implication for prenatal genetic counselling.
Academic Article	Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for "double trouble" overlapping syndromes.
Concept	Heterozygote

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