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Hemoglobin
|
January 1, 1979
Beta 0 thalassemia trait in Sardinia
R Galanello, M A Melis, R Ruggeri, et al.
Journal of Medical Genetics
|
April 1, 1982
Haematological and obstetric aspects of antenatal diagnosis of beta-thalassaemia: experience with 200 cases
A Cao, M Furbetta, A Angius, et al.
Blood
|
March 15, 1991
Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutations
S Murru, G Loudianos, M Deiana, et al.
Journal of Medical Genetics
|
April 1, 1990
Reliability of prenatal diagnosis of genetic diseases by analysis of amplified trophoblast DNA
M C Rosatelli, R Sardu, T Tuveri, et al.
Prenatal Diagnosis
|
October 1, 1994
Improvement of prenatal diagnosis of Wilson disease using microsatellite markers
G Loudianos, A L Figus, A Loi, et al.
Human Genetics
|
December 1, 1996
Wilson disease mutations associated with uncommon haplotypes in Mediterranean patients
G Loudianos, V Dessì, A Angius, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 16, 1999
Visualizing the kinetics of tumor-cell clearance in living animals
T J Sweeney, V Mailänder, A A Tucker, et al.
European Journal of Cancer (Oxford, England : 1990)
|
October 22, 2002
Advancing animal models of neoplasia through in vivo bioluminescence imaging
M Edinger, Y-a Cao, Y S Hornig, et al.
The American Journal of Pediatric Hematology/Oncology
|
January 1, 1983
Effect of subcutaneous desferrioxamine on iron balance in young thalassemia major patients
S De Virgiliis, P Cossu, C Toccafondi, et al.
Cardiologia (Rome, Italy)
|
March 1, 1997
[Does a genetic predisposition for infarction expansion exist? Evaluation of genetic polymorphisms of the renin-angiotensin system]
N Zedda, E Onnis, A Angius, et al.
Page
of 36
Search research articles
Search
Showing results (291-300 of 355) with videos related to
Sort By:
Page
of 36
Hemoglobin
|
January 1, 1979
Beta 0 thalassemia trait in Sardinia
R Galanello, M A Melis, R Ruggeri, et al.
Journal of Medical Genetics
|
April 1, 1982
Haematological and obstetric aspects of antenatal diagnosis of beta-thalassaemia: experience with 200 cases
A Cao, M Furbetta, A Angius, et al.
Blood
|
March 15, 1991
Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutations
S Murru, G Loudianos, M Deiana, et al.
Journal of Medical Genetics
|
April 1, 1990
Reliability of prenatal diagnosis of genetic diseases by analysis of amplified trophoblast DNA
M C Rosatelli, R Sardu, T Tuveri, et al.
Prenatal Diagnosis
|
October 1, 1994
Improvement of prenatal diagnosis of Wilson disease using microsatellite markers
G Loudianos, A L Figus, A Loi, et al.
Human Genetics
|
December 1, 1996
Wilson disease mutations associated with uncommon haplotypes in Mediterranean patients
G Loudianos, V Dessì, A Angius, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 16, 1999
Visualizing the kinetics of tumor-cell clearance in living animals
T J Sweeney, V Mailänder, A A Tucker, et al.
European Journal of Cancer (Oxford, England : 1990)
|
October 22, 2002
Advancing animal models of neoplasia through in vivo bioluminescence imaging
M Edinger, Y-a Cao, Y S Hornig, et al.
The American Journal of Pediatric Hematology/Oncology
|
January 1, 1983
Effect of subcutaneous desferrioxamine on iron balance in young thalassemia major patients
S De Virgiliis, P Cossu, C Toccafondi, et al.
Cardiologia (Rome, Italy)
|
March 1, 1997
[Does a genetic predisposition for infarction expansion exist? Evaluation of genetic polymorphisms of the renin-angiotensin system]
N Zedda, E Onnis, A Angius, et al.
Page
of 36