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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.
Mutagenesis
|
September 10, 2003
Chromosomal aberration frequencies in patients with thalassaemia major undergoing therapy with deferiprone and deferoxamine in a comparative crossover study
R Marshall, F Tricta, R Galanello, 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.
Blood Cells, Molecules & Diseases
|
July 3, 2013
Longitudinal analysis of heart and liver iron in thalassemia major patients according to chelation treatment
F Danjou, R Origa, F Anni, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 1, 1987
The same beta-globin gene mutation is present on nine different beta-thalassemia chromosomes in a Sardinian population
M Pirastu, R Galanello, M A Doherty, et al.
Clinical Genetics
|
July 1, 1984
Control of homozygous beta-thalassemia by carrier screening and antenatal diagnosis in Sardinians
A Cao, L Pintus, U Lecca, et al.
European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies
|
May 1, 1996
Simultaneous automated determination of glucose 6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase activities in whole blood
A Mosca, R Paleari, E Rosti, et al.
British Journal of Haematology
|
April 1, 1980
Interaction between the glucose-6-phosphate dehydrogenase deficiency and thalassaemia genes at phenotype level
G Sanna, F Frau, M A Melis, et al.
British Journal of Haematology
|
December 1, 1983
Phenotypic manifestations of heterozygous non-deletion alpha-thalassaemia (alpha alpha/(alpha alpha)th) in Sardinians
R Galanello, E Paglietti, L Giagu, et al.
European Journal of Pediatrics
|
December 14, 1999
Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome
R Galanello, M D Cipollina, G Carboni, et al.
Page
of 14
Search research articles
Search
Showing results (61-70 of 138) with videos related to
Sort By:
Page
of 14
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.
Mutagenesis
|
September 10, 2003
Chromosomal aberration frequencies in patients with thalassaemia major undergoing therapy with deferiprone and deferoxamine in a comparative crossover study
R Marshall, F Tricta, R Galanello, 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.
Blood Cells, Molecules & Diseases
|
July 3, 2013
Longitudinal analysis of heart and liver iron in thalassemia major patients according to chelation treatment
F Danjou, R Origa, F Anni, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 1, 1987
The same beta-globin gene mutation is present on nine different beta-thalassemia chromosomes in a Sardinian population
M Pirastu, R Galanello, M A Doherty, et al.
Clinical Genetics
|
July 1, 1984
Control of homozygous beta-thalassemia by carrier screening and antenatal diagnosis in Sardinians
A Cao, L Pintus, U Lecca, et al.
European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies
|
May 1, 1996
Simultaneous automated determination of glucose 6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase activities in whole blood
A Mosca, R Paleari, E Rosti, et al.
British Journal of Haematology
|
April 1, 1980
Interaction between the glucose-6-phosphate dehydrogenase deficiency and thalassaemia genes at phenotype level
G Sanna, F Frau, M A Melis, et al.
British Journal of Haematology
|
December 1, 1983
Phenotypic manifestations of heterozygous non-deletion alpha-thalassaemia (alpha alpha/(alpha alpha)th) in Sardinians
R Galanello, E Paglietti, L Giagu, et al.
European Journal of Pediatrics
|
December 14, 1999
Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome
R Galanello, M D Cipollina, G Carboni, et al.
Page
of 14