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S Murru

Showing results (21-30 of 35) with videos related to

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Annali Dell'Istituto Superiore Di Sanita|January 1, 1997
Gestational diabetes: clinical characteristics and birth weightL Volpe, G Di Cianni, P Bottone, et al.
Genomics|September 15, 1994
A DNA fragment from Xq21 replaces a deleted region containing the entire FVIII gene in a severe hemophilia A patientS Murru, L Casula, L Casarino, 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.
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.
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.
Blood|February 1, 1990
Recurrent mutations and three novel rearrangements in the factor VIII gene of hemophilia A patients of Italian descentL Casula, S Murru, M Pecorara, et al.
British Journal of Haematology|February 1, 1992
Promoter mutations producing mild beta-thalassaemia in the Italian populationA Meloni, M C Rosatelli, V Faà, et al.
Blood|March 15, 1991
Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutationsS Murru, G Loudianos, M Deiana, et al.
Blood|March 15, 1990
A spontaneous mutation produced a novel elongated beta-globin chain structural variant (Hb Agnana) with a thalassemia-like phenotypeM S Ristaldi, M Pirastu, S Murru, et al.
British Journal of Haematology|April 1, 1990
The C-T substitution in the distal CACCC box of the beta-globin gene promoter is a common cause of silent beta thalassaemia in the Italian populationM S Ristaldi, S Murru, G Loudianos, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Annali Dell'Istituto Superiore Di Sanita|January 1, 1997
Gestational diabetes: clinical characteristics and birth weightL Volpe, G Di Cianni, P Bottone, et al.
Genomics|September 15, 1994
A DNA fragment from Xq21 replaces a deleted region containing the entire FVIII gene in a severe hemophilia A patientS Murru, L Casula, L Casarino, 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.
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.
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.
Blood|February 1, 1990
Recurrent mutations and three novel rearrangements in the factor VIII gene of hemophilia A patients of Italian descentL Casula, S Murru, M Pecorara, et al.
British Journal of Haematology|February 1, 1992
Promoter mutations producing mild beta-thalassaemia in the Italian populationA Meloni, M C Rosatelli, V Faà, et al.
Blood|March 15, 1991
Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutationsS Murru, G Loudianos, M Deiana, et al.
Blood|March 15, 1990
A spontaneous mutation produced a novel elongated beta-globin chain structural variant (Hb Agnana) with a thalassemia-like phenotypeM S Ristaldi, M Pirastu, S Murru, et al.
British Journal of Haematology|April 1, 1990
The C-T substitution in the distal CACCC box of the beta-globin gene promoter is a common cause of silent beta thalassaemia in the Italian populationM S Ristaldi, S Murru, G Loudianos, et al.
Pageof 4