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Hemoglobin
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January 1, 1995
Molecular basis of alpha-thalassemia in Portugal
M J Peres, L Romão, H Carreiro, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
July 6, 2000
Cystic fibrosis F508del patients have apically localized CFTR in a reduced number of airway cells
D Penque, F Mendes, S Beck, et al.
Thrombosis and Haemostasis
|
November 1, 2000
Ethnic heterogeneity of the factor XIII Val34Leu polymorphism
F A Attié-Castro, M A Zago, J Lavinha, et al.
Human Genetics
|
July 1, 1995
Autosomal dominant polycystic kidney disease: evidence for the existence of a third locus in a Portuguese family
S de Almeida, E de Almeida, D Peters, et al.
Acta Medica Portuguesa
|
April 1, 1996
[Neonatal screening of hemoglobinopathies in a population residing in Portugal]
M J Peres, M H Carreiro, M C Machado, et al.
Blood
|
January 15, 1992
Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin gene
P Moi, G Loudianos, J Lavinha, et al.
Human Genetics
|
July 1, 1992
Novel promoter and splice junction defects add to the genetic, clinical or geographic heterogeneity of beta-thalassaemia in the Portuguese population
P Faustino, L Osório-Almeida, J Barbot, et al.
Human Genetics
|
September 1, 1990
Cystic fibrosis in the Portuguese population: haplotype distribution and molecular pathology
A Duarte, C Barreto, L Marques-Pinto, et al.
Human Biology
|
December 1, 1992
Importation route of the sickle cell trait into Portugal: contribution of molecular epidemiology
J Lavinha, J Gonçalves, P Faustino, et al.
British Journal of Haematology
|
September 1, 1995
Beta-thalassaemia unlinked to the beta-globin gene interacts with sickle-cell trait in a Portuguese family
P Pacheco, M J Peres, P Faustino, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 49) with videos related to
Sort By:
Page
of 5
Hemoglobin
|
January 1, 1995
Molecular basis of alpha-thalassemia in Portugal
M J Peres, L Romão, H Carreiro, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
July 6, 2000
Cystic fibrosis F508del patients have apically localized CFTR in a reduced number of airway cells
D Penque, F Mendes, S Beck, et al.
Thrombosis and Haemostasis
|
November 1, 2000
Ethnic heterogeneity of the factor XIII Val34Leu polymorphism
F A Attié-Castro, M A Zago, J Lavinha, et al.
Human Genetics
|
July 1, 1995
Autosomal dominant polycystic kidney disease: evidence for the existence of a third locus in a Portuguese family
S de Almeida, E de Almeida, D Peters, et al.
Acta Medica Portuguesa
|
April 1, 1996
[Neonatal screening of hemoglobinopathies in a population residing in Portugal]
M J Peres, M H Carreiro, M C Machado, et al.
Blood
|
January 15, 1992
Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin gene
P Moi, G Loudianos, J Lavinha, et al.
Human Genetics
|
July 1, 1992
Novel promoter and splice junction defects add to the genetic, clinical or geographic heterogeneity of beta-thalassaemia in the Portuguese population
P Faustino, L Osório-Almeida, J Barbot, et al.
Human Genetics
|
September 1, 1990
Cystic fibrosis in the Portuguese population: haplotype distribution and molecular pathology
A Duarte, C Barreto, L Marques-Pinto, et al.
Human Biology
|
December 1, 1992
Importation route of the sickle cell trait into Portugal: contribution of molecular epidemiology
J Lavinha, J Gonçalves, P Faustino, et al.
British Journal of Haematology
|
September 1, 1995
Beta-thalassaemia unlinked to the beta-globin gene interacts with sickle-cell trait in a Portuguese family
P Pacheco, M J Peres, P Faustino, et al.
Page
of 5