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M Furbetta

Showing results (11-20 of 32) with videos related to

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British Journal of Haematology|February 1, 1979
Interaction of alpha and beta thalassaemia genes in two Sardinian familiesM Furbetta, R Galanello, A Ximenes, et al.
Journal of Medical Genetics|October 1, 1980
alpha-Thalassaemia in Sardinian infantsR Galanello, G Diana, M Furbetta, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1981
Globin chain synthesis analysis in obligate beta 0-thalassemia heterozygotes with isolated increase of hemoglobin A2 levelsR Galanello, M A Melis, M Furbetta, et al.
Acta Haematologica|January 1, 1980
Hematological characteristics of sardinian alpha-thalassemia carriers detected in a population studyM A Melis, C Rosatelli, A M Falchi, et al.
Journal of Medical Genetics|June 1, 1982
Delta beta (F)-thalassaemia in SardiniaA Cao, M A Melis, R Galanello, et al.
Clinical Genetics|March 1, 1988
Pitfalls in genetic counselling for beta-thalassemia: an individual with 4 different thalassemia mutationsR Galanello, M E Paglietti, M Addis, et al.
British Journal of Haematology|January 1, 1996
A novel mutation (Leu817Pro) causing type 2A von Willebrand diseaseD Gemmati, M L Serino, S Moratelli, et al.
Blood|December 1, 1979
Molecular basis of hemoglobin-H disease in the Mediterranean populationY W Kan, A M Dozy, G Stamatoyannopoulos, et al.
Hemoglobin|January 1, 1981
Diagnosis of the beta 0 thalassemia trait at birthM Furbetta, A Angius, T Tuveri, et al.
Molecular Biology & Medicine|July 1, 1983
Globin gene mapping studies in Sardinian patients homozygous for beta zero ThalassaemiaJ S Wainscoat, J I Bell, J M Old, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
British Journal of Haematology|February 1, 1979
Interaction of alpha and beta thalassaemia genes in two Sardinian familiesM Furbetta, R Galanello, A Ximenes, et al.
Journal of Medical Genetics|October 1, 1980
alpha-Thalassaemia in Sardinian infantsR Galanello, G Diana, M Furbetta, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1981
Globin chain synthesis analysis in obligate beta 0-thalassemia heterozygotes with isolated increase of hemoglobin A2 levelsR Galanello, M A Melis, M Furbetta, et al.
Acta Haematologica|January 1, 1980
Hematological characteristics of sardinian alpha-thalassemia carriers detected in a population studyM A Melis, C Rosatelli, A M Falchi, et al.
Journal of Medical Genetics|June 1, 1982
Delta beta (F)-thalassaemia in SardiniaA Cao, M A Melis, R Galanello, et al.
Clinical Genetics|March 1, 1988
Pitfalls in genetic counselling for beta-thalassemia: an individual with 4 different thalassemia mutationsR Galanello, M E Paglietti, M Addis, et al.
British Journal of Haematology|January 1, 1996
A novel mutation (Leu817Pro) causing type 2A von Willebrand diseaseD Gemmati, M L Serino, S Moratelli, et al.
Blood|December 1, 1979
Molecular basis of hemoglobin-H disease in the Mediterranean populationY W Kan, A M Dozy, G Stamatoyannopoulos, et al.
Hemoglobin|January 1, 1981
Diagnosis of the beta 0 thalassemia trait at birthM Furbetta, A Angius, T Tuveri, et al.
Molecular Biology & Medicine|July 1, 1983
Globin gene mapping studies in Sardinian patients homozygous for beta zero ThalassaemiaJ S Wainscoat, J I Bell, J M Old, et al.
Pageof 4