S. Cacurri

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

B. Brambati, A. Pachì, F. Mangiola, 1999, Neuromuscular Disorders.

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

G. Deidda, L. Felicetti, S. Cacurri, 1996, Journal of medical genetics.

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

P. Grisanti, G. Deidda, E. Vigneti, 1995, European journal of human genetics : EJHG.

4q35 molecular probes for the diagnosis and genetic counseling of facioscapulohumeral muscular dystrophy

G. Deidda, C. Scoppetta, L. Felicetti, 1994, Annals of neurology.

Sequence homology between 4qter and 10qter loci facilitates the instability of subtelomeric KpnI repeat units implicated in facioscapulohumeral muscular dystrophy.

E. Ricci, G. Galluzzi, G. Deidda, 1998, American journal of human genetics.

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

F. Mangiola, P. Tonali, V. Pasceri, 1999, Annals of neurology.

Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral musculatur dystrophy (FSHD)

C. Wijmenga, A. Novelletto, S. Servidei, 1994, Human Genetics.