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M Pirastu

Showing results (71-80 of 101) with videos related to

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Human Genetics|January 1, 1988
Beta-thalassemia mutations in the Portuguese populationM P Gomes, M G da Costa, L B Braga, et al.
Annals of the New York Academy of Sciences|January 1, 1990
Molecular analysis of atypical beta-thalassemia heterozygotesM Pirastu, M S Ristaldi, G Loudianos, et al.
Progress in Clinical and Biological Research|January 1, 1987
Mutations in the A gamma-globin promoter in hereditary persistence of fetal hemoglobin and delta beta zero-thalassemiaS Ottolenghi, B Giglioni, P Comi, et al.
Blood|May 15, 1993
A promoter mutation of the beta-globin gene (-101 C-->T) has an age-related expression patternS Murru, M C Pischedda, A Cao, et al.
Neurology|April 1, 1992
HLA-DQB1 genotype in Sardinian multiple sclerosis: evidence for a key role of DQB1 *0201 and *0302 allelesM G Marrosu, F Muntoni, M R Murru, et al.
Cancer|October 24, 2000
Microsatellite analysis at 10q25-q26 in Sardinian patients with sporadic endometrial carcinoma: identification of specification patterns of genetic alterationG Palmieri, A Manca, A Cossu, et al.
Human Genetics|August 21, 2001
Archival, demographic and genetic studies define a Sardinian sub-isolate as a suitable model for mapping complex traitsA Angius, P M Melis, L Morelli, et al.
Tissue Antigens|July 1, 1991
Different HLA DR2-DQw1 haplotypes in Sardinian and northern Italian populations: implications for multiple sclerosis susceptibilityF Muntoni, M R Murru, G Costa, et al.
Prenatal Diagnosis|October 1, 1994
Improvement of prenatal diagnosis of Wilson disease using microsatellite markersG Loudianos, A L Figus, A Loi, et al.
Human Genetics|December 1, 1996
Wilson disease mutations associated with uncommon haplotypes in Mediterranean patientsG Loudianos, V Dessì, A Angius, et al.
Pageof 11

Showing results (71-80 of 101) with videos related to

Sort By:
Pageof 11
Human Genetics|January 1, 1988
Beta-thalassemia mutations in the Portuguese populationM P Gomes, M G da Costa, L B Braga, et al.
Annals of the New York Academy of Sciences|January 1, 1990
Molecular analysis of atypical beta-thalassemia heterozygotesM Pirastu, M S Ristaldi, G Loudianos, et al.
Progress in Clinical and Biological Research|January 1, 1987
Mutations in the A gamma-globin promoter in hereditary persistence of fetal hemoglobin and delta beta zero-thalassemiaS Ottolenghi, B Giglioni, P Comi, et al.
Blood|May 15, 1993
A promoter mutation of the beta-globin gene (-101 C-->T) has an age-related expression patternS Murru, M C Pischedda, A Cao, et al.
Neurology|April 1, 1992
HLA-DQB1 genotype in Sardinian multiple sclerosis: evidence for a key role of DQB1 *0201 and *0302 allelesM G Marrosu, F Muntoni, M R Murru, et al.
Cancer|October 24, 2000
Microsatellite analysis at 10q25-q26 in Sardinian patients with sporadic endometrial carcinoma: identification of specification patterns of genetic alterationG Palmieri, A Manca, A Cossu, et al.
Human Genetics|August 21, 2001
Archival, demographic and genetic studies define a Sardinian sub-isolate as a suitable model for mapping complex traitsA Angius, P M Melis, L Morelli, et al.
Tissue Antigens|July 1, 1991
Different HLA DR2-DQw1 haplotypes in Sardinian and northern Italian populations: implications for multiple sclerosis susceptibilityF Muntoni, M R Murru, G Costa, et al.
Prenatal Diagnosis|October 1, 1994
Improvement of prenatal diagnosis of Wilson disease using microsatellite markersG Loudianos, A L Figus, A Loi, et al.
Human Genetics|December 1, 1996
Wilson disease mutations associated with uncommon haplotypes in Mediterranean patientsG Loudianos, V Dessì, A Angius, et al.
Pageof 11