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British Journal of Haematology
|
September 1, 1991
Homozygous non-deletion alpha 2 globin gene mutation (initiation codon mutation): clinical and haematological phenotype
R Galanello, M I Monne, L Paderi, et al.
Blood
|
January 15, 1994
Serum erythropoietin and erythropoiesis in high- and low-fetal hemoglobin beta-thalassemia intermedia patients
R Galanello, S Barella, M P Turco, et al.
Annals of the New York Academy of Sciences
|
December 13, 2005
Osteoporosis in beta-thalassemia: Clinical and genetic aspects
R Origa, E Fiumana, M R Gamberini, et al.
British Journal of Haematology
|
December 31, 1997
Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndrome
R Galanello, L Perseu, M A Melis, 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 gene
L Romao, F Cash, I Weiss, et al.
American Journal of Hematology
|
June 1, 1994
Genotype of subjects with borderline hemoglobin A2 levels: implication for beta-thalassemia carrier screening
R Galanello, S Barella, A Ideo, et al.
The Year in Immunology
|
January 1, 1993
Rearrangement of immunoglobin heavy chain constant region in Italian population
U Cariota, A Brusco, C Boccazzi, et al.
The Journal of Automatic Chemistry
|
January 1, 1995
Evaluation of an automatic HPLC analyser for thalassemia and haemoglobin variants screening
R Galanello, S Barella, D Gasperini, et al.
Acta Haematologica
|
January 1, 1992
HbH disease in Sardinia: molecular, hematological and clinical aspects
R Galanello, B Aru, C Dessì, et al.
Human Genetics
|
March 1, 1995
Variability of the immunoglobulin heavy chain constant region locus: a population study
A Brusco, U Cariota, A Bottaro, et al.
Page
of 14
Search research articles
Search
Showing results (111-120 of 138) with videos related to
Sort By:
Page
of 14
British Journal of Haematology
|
September 1, 1991
Homozygous non-deletion alpha 2 globin gene mutation (initiation codon mutation): clinical and haematological phenotype
R Galanello, M I Monne, L Paderi, et al.
Blood
|
January 15, 1994
Serum erythropoietin and erythropoiesis in high- and low-fetal hemoglobin beta-thalassemia intermedia patients
R Galanello, S Barella, M P Turco, et al.
Annals of the New York Academy of Sciences
|
December 13, 2005
Osteoporosis in beta-thalassemia: Clinical and genetic aspects
R Origa, E Fiumana, M R Gamberini, et al.
British Journal of Haematology
|
December 31, 1997
Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndrome
R Galanello, L Perseu, M A Melis, 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 gene
L Romao, F Cash, I Weiss, et al.
American Journal of Hematology
|
June 1, 1994
Genotype of subjects with borderline hemoglobin A2 levels: implication for beta-thalassemia carrier screening
R Galanello, S Barella, A Ideo, et al.
The Year in Immunology
|
January 1, 1993
Rearrangement of immunoglobin heavy chain constant region in Italian population
U Cariota, A Brusco, C Boccazzi, et al.
The Journal of Automatic Chemistry
|
January 1, 1995
Evaluation of an automatic HPLC analyser for thalassemia and haemoglobin variants screening
R Galanello, S Barella, D Gasperini, et al.
Acta Haematologica
|
January 1, 1992
HbH disease in Sardinia: molecular, hematological and clinical aspects
R Galanello, B Aru, C Dessì, et al.
Human Genetics
|
March 1, 1995
Variability of the immunoglobulin heavy chain constant region locus: a population study
A Brusco, U Cariota, A Bottaro, et al.
Page
of 14