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British Medical Journal (Clinical Research Ed.)
|
April 10, 1982
Survival and desferrioxamine in thalassaemia major
B Modell, E A Letsky, D M Flynn, et al.
Annals of the New York Academy of Sciences
|
July 21, 1998
The psychosocial burden of Cooley's anemia in affected children and their parents
N Klein, A Sen, J Rusby, et al.
Scandinavian Journal of Haematology
|
May 1, 1986
Iron chelation using subcutaneous infusions of diethylene triamine penta-acetic acid (DTPA)
M J Pippard, M J Jackson, K Hoffman, et al.
European Journal of Haematology
|
August 1, 1995
Hereditary anaemias and iron deficiency in a tribal population (the Baiga) of central India
P H Reddy, M Petrou, P A Reddy, et al.
BMJ (Clinical Research Ed.)
|
May 15, 2001
Confidential inquiries should be funded in clinical genetics
K Challen, H J Harris, R Harris, et al.
Nature
|
May 15, 1980
Model for antenatal diagnosis of beta-thalassaemia and other monogenic disorders by molecular analysis of linked DNA polymorphisms
P F Little, G Annison, S Darling, et al.
European Journal of Haematology
|
January 1, 1997
Relationship between the severity of beta-thalassaemia syndromes and the number of alleviating mutations
S Ratip, M Petrou, J M Old, et al.
Journal of Community Genetics
|
September 14, 2015
Addressing key issues in the consanguinity-related risk of autosomal recessive disorders in consanguineous communities: lessons from a qualitative study of British Pakistanis
A Darr, N Small, W I U Ahmad, et al.
British Journal of Haematology
|
April 7, 1999
Mapping the prevalence of sickle cell and beta thalassaemia in England: estimating and validating ethnic-specific rates
M Hickman, B Modell, P Greengross, et al.
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]
|
February 1, 1979
Family studies of red-cell metabolism of pyridoxine in beta-thalassaemia
B B Anderson, G M Perry, C B Modell, et al.
Page
of 13
Search research articles
Search
Showing results (81-90 of 126) with videos related to
Sort By:
Page
of 13
British Medical Journal (Clinical Research Ed.)
|
April 10, 1982
Survival and desferrioxamine in thalassaemia major
B Modell, E A Letsky, D M Flynn, et al.
Annals of the New York Academy of Sciences
|
July 21, 1998
The psychosocial burden of Cooley's anemia in affected children and their parents
N Klein, A Sen, J Rusby, et al.
Scandinavian Journal of Haematology
|
May 1, 1986
Iron chelation using subcutaneous infusions of diethylene triamine penta-acetic acid (DTPA)
M J Pippard, M J Jackson, K Hoffman, et al.
European Journal of Haematology
|
August 1, 1995
Hereditary anaemias and iron deficiency in a tribal population (the Baiga) of central India
P H Reddy, M Petrou, P A Reddy, et al.
BMJ (Clinical Research Ed.)
|
May 15, 2001
Confidential inquiries should be funded in clinical genetics
K Challen, H J Harris, R Harris, et al.
Nature
|
May 15, 1980
Model for antenatal diagnosis of beta-thalassaemia and other monogenic disorders by molecular analysis of linked DNA polymorphisms
P F Little, G Annison, S Darling, et al.
European Journal of Haematology
|
January 1, 1997
Relationship between the severity of beta-thalassaemia syndromes and the number of alleviating mutations
S Ratip, M Petrou, J M Old, et al.
Journal of Community Genetics
|
September 14, 2015
Addressing key issues in the consanguinity-related risk of autosomal recessive disorders in consanguineous communities: lessons from a qualitative study of British Pakistanis
A Darr, N Small, W I U Ahmad, et al.
British Journal of Haematology
|
April 7, 1999
Mapping the prevalence of sickle cell and beta thalassaemia in England: estimating and validating ethnic-specific rates
M Hickman, B Modell, P Greengross, et al.
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]
|
February 1, 1979
Family studies of red-cell metabolism of pyridoxine in beta-thalassaemia
B B Anderson, G M Perry, C B Modell, et al.
Page
of 13