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M Pirastu

Showing results (61-70 of 101) with videos related to

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American Journal of Medical Genetics|July 16, 1999
Detection of a rare Wilson disease mutation associated with arylsulfatase A pseudodeficiencyC Battisti, G Loudianos, A Rufa, et al.
Chemical Senses|October 7, 2004
Bitter taste study in a sardinian genetic isolate supports the association of phenylthiocarbamide sensitivity to the TAS2R38 bitter receptor geneD A Prodi, D Drayna, P Forabosco, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 25, 1998
A novel mutation in the GLC1A gene causes juvenile open-angle glaucoma in 4 families from the Italian region of PugliaA Angius, E De Gioia, A Loi, et al.
Blood|April 15, 1990
Deletion delta-thalassemia: the 7.2 kb deletion of Corfu delta beta-thalassemia in a non-beta-thalassemia chromosomeR Galanello, M A Melis, A Podda, et al.
Neurology|November 1, 1988
Sardinian multiple sclerosis is associated with HLA-DR4: a serologic and molecular analysisM G Marrosu, F Muntoni, M R Murru, et al.
Blood|January 15, 1992
Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin geneP Moi, G Loudianos, J Lavinha, et al.
Archives of Neurology|March 1, 1993
Role of predisposing and protective HLA-DQA and HLA-DQB alleles in Sardinian multiple sclerosisM G Marrosu, F Muntoni, M R Murru, et al.
The New England Journal of Medicine|July 2, 1992
Prenatal diagnosis of Wilson's disease by analysis of DNA polymorphismP Cossu, M Pirastu, A Nucaro, et al.
Human Genetics|May 1, 1992
Human alpha-globin gene expression is silenced by terminal truncation of chromosome 16p beginning immediately 3' of the zeta-globin geneL Romao, F Cash, I Weiss, et al.
Hemoglobin|January 1, 1988
Homozygous beta zero-39 mutation with thalassemia intermedia in northern Sardinia: clinical, hematological and molecular analysisL Oggiano, F Dore, P Pistidda, et al.
Pageof 11

Showing results (61-70 of 101) with videos related to

Sort By:
Pageof 11
American Journal of Medical Genetics|July 16, 1999
Detection of a rare Wilson disease mutation associated with arylsulfatase A pseudodeficiencyC Battisti, G Loudianos, A Rufa, et al.
Chemical Senses|October 7, 2004
Bitter taste study in a sardinian genetic isolate supports the association of phenylthiocarbamide sensitivity to the TAS2R38 bitter receptor geneD A Prodi, D Drayna, P Forabosco, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 25, 1998
A novel mutation in the GLC1A gene causes juvenile open-angle glaucoma in 4 families from the Italian region of PugliaA Angius, E De Gioia, A Loi, et al.
Blood|April 15, 1990
Deletion delta-thalassemia: the 7.2 kb deletion of Corfu delta beta-thalassemia in a non-beta-thalassemia chromosomeR Galanello, M A Melis, A Podda, et al.
Neurology|November 1, 1988
Sardinian multiple sclerosis is associated with HLA-DR4: a serologic and molecular analysisM G Marrosu, F Muntoni, M R Murru, et al.
Blood|January 15, 1992
Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin geneP Moi, G Loudianos, J Lavinha, et al.
Archives of Neurology|March 1, 1993
Role of predisposing and protective HLA-DQA and HLA-DQB alleles in Sardinian multiple sclerosisM G Marrosu, F Muntoni, M R Murru, et al.
The New England Journal of Medicine|July 2, 1992
Prenatal diagnosis of Wilson's disease by analysis of DNA polymorphismP Cossu, M Pirastu, A Nucaro, et al.
Human Genetics|May 1, 1992
Human alpha-globin gene expression is silenced by terminal truncation of chromosome 16p beginning immediately 3' of the zeta-globin geneL Romao, F Cash, I Weiss, et al.
Hemoglobin|January 1, 1988
Homozygous beta zero-39 mutation with thalassemia intermedia in northern Sardinia: clinical, hematological and molecular analysisL Oggiano, F Dore, P Pistidda, et al.
Pageof 11