Universidade Federal de São Paulo, Discipline Hematol & Transfus Med, BR-04023092 São Paulo, BrazilUniversidade Federal de São Paulo, Discipline Hematol & Transfus Med, BR-04023092 São Paulo, BrazilWeb of Scienc
The 22 antigens of the Kell blood group system are located on a red blood cell (RBC) membrane glycop...
In this study, we report on 8 compound heterozygotes for mutations in the key erythroid transcriptio...
BACKGROUND: Red blood group genes are highly polymorphic and the distribution of alleles varies amon...
Background: The Kell blood group system expresses high and low frequency antigens with the most impo...
Background: Pyruvate kinase deficiency is a hereditary disease that affects the glycolytic pathway o...
BACKGROUND: The Kell blood group system expresses high and low frequency antigens with the most impo...
Tese de doutoramento em Antropologia (Antropologia Biológica) apresentada à Faculdade de Ciências e ...
We established the molecular basis for pyruvate kinase (PK) deficiency in a white male patient with ...
This work analyses the results of research regarding the predisposition of genetic hematological ris...
International audienceINTRODUCTION:Pyruvate kinase (PK) deficiency is one of the most common heredit...
Introduction: It is mandatory that every blood donor must have their haemoglobin (Hb) values measure...
DNA analysis was performed on 30 unrelated patients with hereditary nonspherocytic hemolytic anemia ...
AbstractBackgroundRed blood cell genes are highly polymorphic with the distribution of alleles varyi...
[No abstract available]54821282129Lee, S., Russo, D., Redman, C., Functional and structural aspects ...
The prevalence of the prothrombin gene variant (allele 20.210 A), factor V Leiden mutation, and homo...
The 22 antigens of the Kell blood group system are located on a red blood cell (RBC) membrane glycop...
In this study, we report on 8 compound heterozygotes for mutations in the key erythroid transcriptio...
BACKGROUND: Red blood group genes are highly polymorphic and the distribution of alleles varies amon...
Background: The Kell blood group system expresses high and low frequency antigens with the most impo...
Background: Pyruvate kinase deficiency is a hereditary disease that affects the glycolytic pathway o...
BACKGROUND: The Kell blood group system expresses high and low frequency antigens with the most impo...
Tese de doutoramento em Antropologia (Antropologia Biológica) apresentada à Faculdade de Ciências e ...
We established the molecular basis for pyruvate kinase (PK) deficiency in a white male patient with ...
This work analyses the results of research regarding the predisposition of genetic hematological ris...
International audienceINTRODUCTION:Pyruvate kinase (PK) deficiency is one of the most common heredit...
Introduction: It is mandatory that every blood donor must have their haemoglobin (Hb) values measure...
DNA analysis was performed on 30 unrelated patients with hereditary nonspherocytic hemolytic anemia ...
AbstractBackgroundRed blood cell genes are highly polymorphic with the distribution of alleles varyi...
[No abstract available]54821282129Lee, S., Russo, D., Redman, C., Functional and structural aspects ...
The prevalence of the prothrombin gene variant (allele 20.210 A), factor V Leiden mutation, and homo...
The 22 antigens of the Kell blood group system are located on a red blood cell (RBC) membrane glycop...
In this study, we report on 8 compound heterozygotes for mutations in the key erythroid transcriptio...
BACKGROUND: Red blood group genes are highly polymorphic and the distribution of alleles varies amon...