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G Deidda

Showing results (11-20 of 24) with videos related to

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Haematologica|May 1, 1997
Silent thalassemias: genotypes and phenotypesI Bianco, M P Cappabianca, E Foglietta, et al.
Human Genetics|October 1, 1994
Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD)S Cacurri, G Deidda, N Piazzo, et al.
Human Molecular Genetics|November 25, 2000
Interchromosomal repeat array interactions between chromosomes 4 and 10: a model for subtelomeric plasticityP G van Overveld, R J Lemmers, G Deidda, et al.
Journal of Medical Genetics|April 3, 2004
FRG1P is localised in the nucleolus, Cajal bodies, and specklesS van Koningsbruggen, R W Dirks, A M Mommaas, et al.
Human Genetics|August 1, 1990
Molecular characterization of beta-thalassemia mutations in EgyptA Novelletto, M Hafez, G Deidda, et al.
Haematologica|January 4, 1998
Phenotypes of individuals with a beta thal classical allele associated either with a beta thal silent allele or with alpha globin gene triplicationI Bianco, M Lerone, E Foglietta, et al.
Human Genetics|February 1, 1989
Frequency and molecular types of deletional alpha-thalassemia in EgyptA Novelletto, M Hafez, A Di Rienzo, et al.
Neuromuscular Disorders : NMD|June 26, 1999
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 diseaseG Galluzzi, G Deidda, S Cacurri, et al.
Journal of Medical Genetics|November 2, 1999
A new dosage test for subtelomeric 4;10 translocations improves conventional diagnosis of facioscapulohumeral muscular dystrophy (FSHD)S M van der Maarel, G Deidda, R J Lemmers, et al.
Annals of Neurology|June 9, 1999
Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotypeE Ricci, G Galluzzi, G Deidda, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Haematologica|May 1, 1997
Silent thalassemias: genotypes and phenotypesI Bianco, M P Cappabianca, E Foglietta, et al.
Human Genetics|October 1, 1994
Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD)S Cacurri, G Deidda, N Piazzo, et al.
Human Molecular Genetics|November 25, 2000
Interchromosomal repeat array interactions between chromosomes 4 and 10: a model for subtelomeric plasticityP G van Overveld, R J Lemmers, G Deidda, et al.
Journal of Medical Genetics|April 3, 2004
FRG1P is localised in the nucleolus, Cajal bodies, and specklesS van Koningsbruggen, R W Dirks, A M Mommaas, et al.
Human Genetics|August 1, 1990
Molecular characterization of beta-thalassemia mutations in EgyptA Novelletto, M Hafez, G Deidda, et al.
Haematologica|January 4, 1998
Phenotypes of individuals with a beta thal classical allele associated either with a beta thal silent allele or with alpha globin gene triplicationI Bianco, M Lerone, E Foglietta, et al.
Human Genetics|February 1, 1989
Frequency and molecular types of deletional alpha-thalassemia in EgyptA Novelletto, M Hafez, A Di Rienzo, et al.
Neuromuscular Disorders : NMD|June 26, 1999
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 diseaseG Galluzzi, G Deidda, S Cacurri, et al.
Journal of Medical Genetics|November 2, 1999
A new dosage test for subtelomeric 4;10 translocations improves conventional diagnosis of facioscapulohumeral muscular dystrophy (FSHD)S M van der Maarel, G Deidda, R J Lemmers, et al.
Annals of Neurology|June 9, 1999
Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotypeE Ricci, G Galluzzi, G Deidda, et al.
Pageof 3