At position 0.5 kb upstream to the &globin gene lies a repeated purine-pyrimidine sequence (AT),(T),, which exhibits a great vari-ation in length and configuration. ’ The different specific patterns of this sequence are in strict linkage disequilibrium with the 0-globin haplotype. The (AT)yT5 motif has been identified several years ago in a carrier of silent 0-thalassemia of Albanian descent. ’ Later on a number of studies have confirmed the association between the (AT),TS motif and silent 8-thalassemia ’ and showed the presence of the same motif in cis to the S mutation in Indian AS heterozygotes, who are char-acterized by a consistently lower expression of HbS compared with African AS carriers4 The (AT),(T), sequence lies within a neg...
The hypothesis that three separate mutations to the Β S -globin gene have occurred in Africa in chal...
Sickle cell hemoglobin is a b chain structural variant where valine is substituted for glutamic acid...
Summary: A single nucleotide substitution and the effect on the phenotype in an Indonesian family wi...
Approximately 60 % of the y-globin chains of adults are 5-globin chains. Reduced proportions of &apo...
[No abstract available]893273275Ho, P.J., Rochette, J., Fisher, C.A., Wonke, B., Jarvis, M.K., Yardu...
Genetic variation at the human a-globin gene complex has only been characterised to date ...
To the Editor: peak (p”) eluting after the normal PA chain (Fig 1A). The total radioactivity of dPA ...
Although δ-globin gene (HBD MIM#142000) mutations have no clinical implications, co-inheritance of β...
<p>The data were collected from HbVar, the globin gene server <a href="http://globin.cse.psu.edu/glo...
We have cloned the single p-globin gene from an Italian patient who is a double heterozygote for (3°...
?-Globin haplotypes have been used to investigate the origin and spread of ?-globin mutations such a...
The silent carrier of (beta) thalassemia has a decreased (beta)/(alpha) globin synthesis ratio, but ...
The proposita in a Sudanese family had a moderately severe thalassemia syndrome with the hemoglobin ...
Objectives: Alpha (α) and beta (β) thalassemia are the most prevalent genetic hematological disorder...
Introduction: Interactions of different hemoglobin variants with thalassemia alleles can result in ...
The hypothesis that three separate mutations to the Β S -globin gene have occurred in Africa in chal...
Sickle cell hemoglobin is a b chain structural variant where valine is substituted for glutamic acid...
Summary: A single nucleotide substitution and the effect on the phenotype in an Indonesian family wi...
Approximately 60 % of the y-globin chains of adults are 5-globin chains. Reduced proportions of &apo...
[No abstract available]893273275Ho, P.J., Rochette, J., Fisher, C.A., Wonke, B., Jarvis, M.K., Yardu...
Genetic variation at the human a-globin gene complex has only been characterised to date ...
To the Editor: peak (p”) eluting after the normal PA chain (Fig 1A). The total radioactivity of dPA ...
Although δ-globin gene (HBD MIM#142000) mutations have no clinical implications, co-inheritance of β...
<p>The data were collected from HbVar, the globin gene server <a href="http://globin.cse.psu.edu/glo...
We have cloned the single p-globin gene from an Italian patient who is a double heterozygote for (3°...
?-Globin haplotypes have been used to investigate the origin and spread of ?-globin mutations such a...
The silent carrier of (beta) thalassemia has a decreased (beta)/(alpha) globin synthesis ratio, but ...
The proposita in a Sudanese family had a moderately severe thalassemia syndrome with the hemoglobin ...
Objectives: Alpha (α) and beta (β) thalassemia are the most prevalent genetic hematological disorder...
Introduction: Interactions of different hemoglobin variants with thalassemia alleles can result in ...
The hypothesis that three separate mutations to the Β S -globin gene have occurred in Africa in chal...
Sickle cell hemoglobin is a b chain structural variant where valine is substituted for glutamic acid...
Summary: A single nucleotide substitution and the effect on the phenotype in an Indonesian family wi...