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G P Tamagnini

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Hemoglobin|May 1, 1997

Hemoglobin disorders in MacaoM L Ribeiro, G P Tamagnini

Hemoglobin|January 1, 1988

Congenital anemias in MacauG P Tamagnini, B Kuam, W K Fai

Lancet (London, England)|July 26, 1975

Letter: Factor-VIII concentrate in haemophiliaG P Tamagnini, K M Dormandy, D Ellis, et al.

Thrombosis and Haemostasis|July 29, 1984

Congenital deficiency of vitamin K-dependent coagulation factors and protein CV Vicente, R Maia, I Alberca, et al.

British Journal of Haematology|June 1, 1983

Beta + thalassemia--Portuguese type: clinical, haematological and molecular studies of a newly defined form of beta thalassaemiaG P Tamagnini, M C Lopes, M E Castanheira, et al.

British Journal of Haematology|October 1, 1991

Dominant beta-thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the beta-globin geneR Oner, C Oner, J B Wilson, et al.

Hemoglobin|March 18, 2000

Hb Vila Real [beta36(C2)Pro-->His]: a newly discovered high oxygen affinity variantM C Bento, M L Ribeiro, E Cunha, et al.

British Journal of Haematology|April 1, 1992

A novel beta zero-thalassaemia mutation (codon 15, TGG----TGA) is prevalent in a population of central PortugalM L Ribeiro, E Baysal, F Kutlar, et al.

Hemoglobin|February 1, 1993

Beta-thalassemia mutations in the Portuguese; high frequencies of two alleles in restricted populationsG P Tamagnini, P Gonçalves, M L Ribeiro, et al.

Hemoglobin|January 1, 1990

Hb Hekinan observed in three Chinese from Macau; identification of the GAG----GAT mutation in the alpha 1-globin geneW Zhao, J B Wilson, B B Webber, et al.

Pageof 2

Search research articles

Showing results (1-10 of 13) with videos related to

Sort By:

Pageof 2

Hemoglobin|May 1, 1997

Hemoglobin disorders in MacaoM L Ribeiro, G P Tamagnini

Hemoglobin|January 1, 1988

Congenital anemias in MacauG P Tamagnini, B Kuam, W K Fai

Lancet (London, England)|July 26, 1975

Letter: Factor-VIII concentrate in haemophiliaG P Tamagnini, K M Dormandy, D Ellis, et al.

Thrombosis and Haemostasis|July 29, 1984

Congenital deficiency of vitamin K-dependent coagulation factors and protein CV Vicente, R Maia, I Alberca, et al.

British Journal of Haematology|June 1, 1983

Beta + thalassemia--Portuguese type: clinical, haematological and molecular studies of a newly defined form of beta thalassaemiaG P Tamagnini, M C Lopes, M E Castanheira, et al.

British Journal of Haematology|October 1, 1991

Dominant beta-thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the beta-globin geneR Oner, C Oner, J B Wilson, et al.

Hemoglobin|March 18, 2000

Hb Vila Real [beta36(C2)Pro-->His]: a newly discovered high oxygen affinity variantM C Bento, M L Ribeiro, E Cunha, et al.

British Journal of Haematology|April 1, 1992

A novel beta zero-thalassaemia mutation (codon 15, TGG----TGA) is prevalent in a population of central PortugalM L Ribeiro, E Baysal, F Kutlar, et al.

Hemoglobin|February 1, 1993

Beta-thalassemia mutations in the Portuguese; high frequencies of two alleles in restricted populationsG P Tamagnini, P Gonçalves, M L Ribeiro, et al.

Hemoglobin|January 1, 1990

Hb Hekinan observed in three Chinese from Macau; identification of the GAG----GAT mutation in the alpha 1-globin geneW Zhao, J B Wilson, B B Webber, et al.

Pageof 2