Few studies have described the dynamics of haemoglobin production in African populations with a high prevalence of haemoglobinopathies. We have used the BioRad Variant ClassicTM HPLC method to document the production patterns of the common haemoglobin variants HbA, HbA2, HbF and HbS, stratified by a+thalassaemia genotype, among 15,301 infants recruited to a study on the Coast of Kenya. Notably, we confirm that HbA2 measurements determined using this instrument are unreliable in HbAS and HbSS subjects. Further, we showed that HbA2 exceeded 4.0%, a level consistent with the presence of a-thalassaemia, in 0.8% of infants of HbAA phenotype who participated in our study. a-thalassaemia, has not been widely reported in the East Africa region and,...
Purpose Our objective was to compare observed and expected genotype proportions from newborn screeni...
Information on the etiology of anemia is necessary to design effective anemia control programs. Our ...
COMPETE 2020. POCI-01-0145-FEDER-007274 to i3S.Mutations on the HBB gene are a common cause of hemog...
Few studies have described the dynamics of haemoglobin production in African populations with a high...
Background β-Thalassemia is rare in sub-Saharan Africa. Previous studies have suggested that it is l...
The bloods of 1800 western Kenyans were screened for hemoglobin variants by electrophoresis on cellu...
Haemoglobin C (HbC) is one of the commonest structural haemoglobin variants in human populations. Al...
Based in the parish of Manchester in central Jamaica, the Manchester Project offered free detection ...
We evaluated the use of an HPLC method for screening hemoglobins in cord blood. We studied the genot...
Purpose: Our objective was to compare observed and expected genotype proportions from newborn screen...
Although inherited blood disorders are common among children in many parts of Africa, limited data a...
Our objective was to compare observed and expected genotype proportions from newborn screening surve...
We evaluated the use of an HPLC method for screening hemoglobins in cord blood. We studied the genot...
Cellulose acetate electrophoresis technique has been used to estimate haemoglobin genotyp...
The alpha+ thalassaemias are the most common single gene disorders of humans, yet little is known ab...
Purpose Our objective was to compare observed and expected genotype proportions from newborn screeni...
Information on the etiology of anemia is necessary to design effective anemia control programs. Our ...
COMPETE 2020. POCI-01-0145-FEDER-007274 to i3S.Mutations on the HBB gene are a common cause of hemog...
Few studies have described the dynamics of haemoglobin production in African populations with a high...
Background β-Thalassemia is rare in sub-Saharan Africa. Previous studies have suggested that it is l...
The bloods of 1800 western Kenyans were screened for hemoglobin variants by electrophoresis on cellu...
Haemoglobin C (HbC) is one of the commonest structural haemoglobin variants in human populations. Al...
Based in the parish of Manchester in central Jamaica, the Manchester Project offered free detection ...
We evaluated the use of an HPLC method for screening hemoglobins in cord blood. We studied the genot...
Purpose: Our objective was to compare observed and expected genotype proportions from newborn screen...
Although inherited blood disorders are common among children in many parts of Africa, limited data a...
Our objective was to compare observed and expected genotype proportions from newborn screening surve...
We evaluated the use of an HPLC method for screening hemoglobins in cord blood. We studied the genot...
Cellulose acetate electrophoresis technique has been used to estimate haemoglobin genotyp...
The alpha+ thalassaemias are the most common single gene disorders of humans, yet little is known ab...
Purpose Our objective was to compare observed and expected genotype proportions from newborn screeni...
Information on the etiology of anemia is necessary to design effective anemia control programs. Our ...
COMPETE 2020. POCI-01-0145-FEDER-007274 to i3S.Mutations on the HBB gene are a common cause of hemog...