Giancarlo Deidda

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 · 296 citations

Ecori Fragment Size, Rare Diseases, Facioscapulohumeral Muscular Dystrophy +15

De Novo Facioscapulohumeral Muscular Dystrophy: Frequent Somatic Mosaicism, Sex-Dependent Phenotype, and the Role of Mitotic Transchromosomal Repeat Interaction between Chromosomes 4 and 10

Silvère M. van der Maarel, Giancarlo Deidda, Richard J.L.F. Lemmers et al. · The American Journal of Human Genetics · 2000 · 162 citations · Full text

Chromatin, Developmental Biology, Mendelian Disorder +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 · 142 citations · Full text

Genetic Analysis, Facioscapulohumeral Muscular Dystrophy, Allelic Variant +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 · 102 citations

Biology, Chromosome Dynamics, Genetic Disorder +8

Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2

Patrizia Calandra, Isabella Cascino, Richard J.L.F. Lemmers et al. · Journal of Medical Genetics · 2016 · 71 citations