S. Cacurri

Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number ofKpnI repeats at the 4q35 locus and clinical phenotype

Enzo Ricci, Giuliana Galluzzi, Giancarlo Deidda et al. · Annals of Neurology · 1999 · 301 citations

Life Sciences, Genetics, Molecular Genetics +12

Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD).

Giancarlo Deidda, S. Cacurri, N. Piazzo et al. · Journal of Medical Genetics · 1996 · 144 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Physical Mapping Evidence for a Duplicated Region on Chromosome 10qter Showing High Homology with the Facioscapulohumeral Muscular Dystrophy Locus on Chromosome 4qter

Giancarlo Deidda, S. Cacurri, Paola Grisanti et al. · European Journal of Human Genetics · 1995 · 104 citations

Life Sciences, Genetics, Molecular Genetics +12

Sequence Homology between 4qter and 10qter Loci Facilitates the Instability of Subtelomeric KpnI Repeat Units Implicated in Facioscapulohumeral Muscular Dystrophy

S. Cacurri, N. Piazzo, Giancarlo Deidda et al. · The American Journal of Human Genetics · 1998 · 58 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Molecular analysis of 4q35 rearrangements in facioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease

Giuliana Galluzzi, Giancarlo Deidda, S. Cacurri et al. · Neuromuscular Disorders · 1999 · 27 citations

Life Sciences, Genetics, Molecular Genetics +13