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	1.	Sequence homology between 4qter and 10qter loci facilitates the instability of subtelomeric KpnI repeat units implicated in facioscapulohumeral muscular dystrophy. [electronic resource] by Cacurri, S Piazzo, N Deidda, G Vigneti, E Galluzzi, G Colantoni, L Merico, B Ricci, E Felicetti, L Producer: 19980813 In: American journal of human genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Molecular analysis of 4q35 rearrangements in fascioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease. [electronic resource] by Galluzzi, G Deidda, G Cacurri, S Colantoni, L Piazzo, N Vigneti, E Ricci, E Servidei, S Merico, B Pachì, A Brambati, B Mangiola, F Tonali, P Felicetti, L Producer: 19990811 In: Neuromuscular disorders : NMD vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype. [electronic resource] by Ricci, E Galluzzi, G Deidda, G Cacurri, S Colantoni, L Merico, B Piazzo, N Servidei, S Vigneti, E Pasceri, V Silvestri, G Mirabella, M Mangiola, F Tonali, P Felicetti, L Producer: 19990624 In: Annals of neurology vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)