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British Journal of Haematology
|
May 1, 1993
Normal individuals with high Hb A2 levels
D Gasperini, A Cao, L Paderi, et al.
British Journal of Haematology
|
February 15, 2002
Cholelithiasis and Gilbert's syndrome in homozygous beta-thalassaemia
R Galanello, S Piras, S Barella, et al.
American Journal of Hematology
|
October 1, 1988
Interaction of heterozygous beta zero-thalassemia with single functional alpha-globin gene
R Galanello, E Paglietti, M A Melis, et al.
British Journal of Haematology
|
June 1, 1995
A promoter mutation, C-->T at position -92, leading to silent beta-thalassaemia
M C Rosatelli, V Faà, A Meloni, et al.
British Journal of Haematology
|
August 1, 1989
Erythropoiesis following bone marrow transplantation from donors heterozygous for beta-thalassaemia
R Galanello, S Barella, L Maccioni, et al.
Haematologica
|
November 1, 1994
Interferon-alpha 2a therapy in CML: disappearance of BCR/ABL transcript in a case of long-lasting continuous cytogenetic conversion
S Pardini, M Addis, F Dore, et al.
American Journal of Hematology
|
January 1, 1992
Heterozygous beta-thalassemia: relationship between the hematological phenotype and the type of beta-thalassemia mutation
C Rosatelli, G B Leoni, T Tuveri, et al.
Hemoglobin
|
January 1, 1997
Hb Puttelange [beta 140(H19)Ala-->Val] in an Italian man with polycythemia
R Galanello, R Paleari, L Perseu, et al.
Clinical Genetics
|
November 1, 1990
Fetal hydrops in Sardinia: implications for genetic counselling
R Galanello, M A Sanna, L Maccioni, et al.
American Journal of Hematology
|
January 10, 1998
Heterozygous beta-thalassemia with thalassemia intermedia phenotype
D Gasperini, L Perseu, M A Melis, et al.
Page
of 14
Search research articles
Search
Showing results (91-100 of 138) with videos related to
Sort By:
Page
of 14
British Journal of Haematology
|
May 1, 1993
Normal individuals with high Hb A2 levels
D Gasperini, A Cao, L Paderi, et al.
British Journal of Haematology
|
February 15, 2002
Cholelithiasis and Gilbert's syndrome in homozygous beta-thalassaemia
R Galanello, S Piras, S Barella, et al.
American Journal of Hematology
|
October 1, 1988
Interaction of heterozygous beta zero-thalassemia with single functional alpha-globin gene
R Galanello, E Paglietti, M A Melis, et al.
British Journal of Haematology
|
June 1, 1995
A promoter mutation, C-->T at position -92, leading to silent beta-thalassaemia
M C Rosatelli, V Faà, A Meloni, et al.
British Journal of Haematology
|
August 1, 1989
Erythropoiesis following bone marrow transplantation from donors heterozygous for beta-thalassaemia
R Galanello, S Barella, L Maccioni, et al.
Haematologica
|
November 1, 1994
Interferon-alpha 2a therapy in CML: disappearance of BCR/ABL transcript in a case of long-lasting continuous cytogenetic conversion
S Pardini, M Addis, F Dore, et al.
American Journal of Hematology
|
January 1, 1992
Heterozygous beta-thalassemia: relationship between the hematological phenotype and the type of beta-thalassemia mutation
C Rosatelli, G B Leoni, T Tuveri, et al.
Hemoglobin
|
January 1, 1997
Hb Puttelange [beta 140(H19)Ala-->Val] in an Italian man with polycythemia
R Galanello, R Paleari, L Perseu, et al.
Clinical Genetics
|
November 1, 1990
Fetal hydrops in Sardinia: implications for genetic counselling
R Galanello, M A Sanna, L Maccioni, et al.
American Journal of Hematology
|
January 10, 1998
Heterozygous beta-thalassemia with thalassemia intermedia phenotype
D Gasperini, L Perseu, M A Melis, et al.
Page
of 14