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A Melis

Showing results (101-110 of 171) with videos related to

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Human Mutation|January 8, 2000
A new glucose 6 phosphate dehydrogenase variant G6PD Sinnai (34 G-->T). Mutations in brief no. 156. OnlineR Galanello, D Loi, C Sollaino, et al.
Hemoglobin|January 1, 1978
Hemoglobin H disease in Sardinia: phenotypic and genetic observationsR Galanello, M A Melis, M Furbetta, et al.
Blood|November 1, 1983
A family with segregating triplicated alpha globin loci and beta thalassemiaR Galanello, R Ruggeri, E Paglietti, et al.
Clinical Genetics|August 28, 2007
Frequency of hemochromatosis gene (HFE) mutations in Corsica (France)I Piras, A Melis, A Falchi, et al.
Acta Haematologica|January 1, 1983
Serum ferritin levels in hemoglobin H diseaseR Galanello, M A Melis, E Paglietti, et al.
American Journal of Medical Genetics. Part A|June 11, 2005
New case of contiguous gene syndrome at chromosome 8p11.2p12M Cau, R Congiu, R Origa, et al.
Annali Di Igiene : Medicina Preventiva E Di Comunita|September 1, 1990
[Prevalence of hepatitis virus (HBV and HCV) and HIV-1 infections in a prison community]G Pinducciu, M Arnone, G Piu, et al.
Haematologica|May 1, 1985
Hematological phenotype of carriers of deletion alpha-thalassemia according to the alpha-globin genotypeR Galanello, E Paglietti, N Giagu, et al.
European Neurology|January 1, 1992
Polymerase chain reaction analysis for specific HTLV-1 sequences from cerebrospinal fluid and peripheral blood cells in Sardinian multiple sclerosis patientsM G Marrosu, A P Mazzoleni, S Galantuomo, et al.
Research Communications in Chemical Pathology and Pharmacology|April 1, 1991
Occupational exposure to lead and blood cholesterol in glucose-6-phosphate dehydrogenase deficient and normal subjectsP L Cocco, E Cocco, M S Anni, et al.
Pageof 18

Showing results (101-110 of 171) with videos related to

Sort By:
Pageof 18
Human Mutation|January 8, 2000
A new glucose 6 phosphate dehydrogenase variant G6PD Sinnai (34 G-->T). Mutations in brief no. 156. OnlineR Galanello, D Loi, C Sollaino, et al.
Hemoglobin|January 1, 1978
Hemoglobin H disease in Sardinia: phenotypic and genetic observationsR Galanello, M A Melis, M Furbetta, et al.
Blood|November 1, 1983
A family with segregating triplicated alpha globin loci and beta thalassemiaR Galanello, R Ruggeri, E Paglietti, et al.
Clinical Genetics|August 28, 2007
Frequency of hemochromatosis gene (HFE) mutations in Corsica (France)I Piras, A Melis, A Falchi, et al.
Acta Haematologica|January 1, 1983
Serum ferritin levels in hemoglobin H diseaseR Galanello, M A Melis, E Paglietti, et al.
American Journal of Medical Genetics. Part A|June 11, 2005
New case of contiguous gene syndrome at chromosome 8p11.2p12M Cau, R Congiu, R Origa, et al.
Annali Di Igiene : Medicina Preventiva E Di Comunita|September 1, 1990
[Prevalence of hepatitis virus (HBV and HCV) and HIV-1 infections in a prison community]G Pinducciu, M Arnone, G Piu, et al.
Haematologica|May 1, 1985
Hematological phenotype of carriers of deletion alpha-thalassemia according to the alpha-globin genotypeR Galanello, E Paglietti, N Giagu, et al.
European Neurology|January 1, 1992
Polymerase chain reaction analysis for specific HTLV-1 sequences from cerebrospinal fluid and peripheral blood cells in Sardinian multiple sclerosis patientsM G Marrosu, A P Mazzoleni, S Galantuomo, et al.
Research Communications in Chemical Pathology and Pharmacology|April 1, 1991
Occupational exposure to lead and blood cholesterol in glucose-6-phosphate dehydrogenase deficient and normal subjectsP L Cocco, E Cocco, M S Anni, et al.
Pageof 18