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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. Online
R Galanello, D Loi, C Sollaino, et al.
Hemoglobin
|
January 1, 1978
Hemoglobin H disease in Sardinia: phenotypic and genetic observations
R Galanello, M A Melis, M Furbetta, et al.
Blood
|
November 1, 1983
A family with segregating triplicated alpha globin loci and beta thalassemia
R 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 disease
R 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 8p11.2p12
M 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 genotype
R 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 patients
M 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 subjects
P L Cocco, E Cocco, M S Anni, et al.
Page
of 18
Search research articles
Search
Showing results (101-110 of 171) with videos related to
Sort By:
Page
of 18
Human Mutation
|
January 8, 2000
A new glucose 6 phosphate dehydrogenase variant G6PD Sinnai (34 G-->T). Mutations in brief no. 156. Online
R Galanello, D Loi, C Sollaino, et al.
Hemoglobin
|
January 1, 1978
Hemoglobin H disease in Sardinia: phenotypic and genetic observations
R Galanello, M A Melis, M Furbetta, et al.
Blood
|
November 1, 1983
A family with segregating triplicated alpha globin loci and beta thalassemia
R 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 disease
R 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 8p11.2p12
M 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 genotype
R 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 patients
M 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 subjects
P L Cocco, E Cocco, M S Anni, et al.
Page
of 18