We have examined the molecular structure of the human alpha globin gene complex from individuals with a common form of alpha thalassaemia in which one of the duplicated pair of alpha genes (alpha alpha) has been deleted (-alpha 3-7). Restriction mapping and DNA sequence analysis of the mutants indicate that different -alpha 3.7 chromosomes are the result of at least three independent events. In each case the genetic crossover has occurred within a region of complete homology between the alpha 1 and alpha 2 genes. Since the -alpha chromosomes may reflect the processes of crossover fixation and gene conversion between the two genes, their structures may provide some insight into the mechanism by which the concerted evolution of the human alph...
In alpha-thalassemia, the genetic locus for the alpha chains of adult hemoglobin is not expressed. W...
Most cases of {alpha}-thalassemia result from large deletions at the {alpha}-globin locus (1). The {...
Alpha-thalassemia is an inherited hemoglobin disorder characterized by a microcytic hypochromic anem...
The human α-globin gene complex on chromosome 16 consists of two adult α genes (α1 and α2) separated...
The complete nucleotide sequence of a human alpha-globin pseudogene (psi alpha 1) is presented. Comp...
The clinical diversity of thalassemia depends on interaction of diverse genetic defects. We have cha...
We describe a family in which alpha-thalassemia occurs in association with a deletion of 62 kilobase...
We have sequenced and fully annotated a 65,871-bp region of mouse Chromosome 17 including the Hba-ps...
We have sequenced and fully annotated a 65,871-bp region of mouse Chromosome 17 including the Hba-ps...
This work comprises two parts: the molecular characterization of two cases of hemoglobin H disease a...
We have characterized a newly identified 16.6 kb deletion which removes a significant proportion of ...
DNA analysis of the alpha- and beta-globin gene clusters has revealed substantial variability betwee...
We have characterized a newly identified 16.6 kb deletion which removes a significant proportion of ...
In alpha-thalassemia, the genetic locus for the alpha chains of adult hemoglobin is not expressed. W...
Genetic variation at the human a-globin gene complex has only been characterised to date ...
In alpha-thalassemia, the genetic locus for the alpha chains of adult hemoglobin is not expressed. W...
Most cases of {alpha}-thalassemia result from large deletions at the {alpha}-globin locus (1). The {...
Alpha-thalassemia is an inherited hemoglobin disorder characterized by a microcytic hypochromic anem...
The human α-globin gene complex on chromosome 16 consists of two adult α genes (α1 and α2) separated...
The complete nucleotide sequence of a human alpha-globin pseudogene (psi alpha 1) is presented. Comp...
The clinical diversity of thalassemia depends on interaction of diverse genetic defects. We have cha...
We describe a family in which alpha-thalassemia occurs in association with a deletion of 62 kilobase...
We have sequenced and fully annotated a 65,871-bp region of mouse Chromosome 17 including the Hba-ps...
We have sequenced and fully annotated a 65,871-bp region of mouse Chromosome 17 including the Hba-ps...
This work comprises two parts: the molecular characterization of two cases of hemoglobin H disease a...
We have characterized a newly identified 16.6 kb deletion which removes a significant proportion of ...
DNA analysis of the alpha- and beta-globin gene clusters has revealed substantial variability betwee...
We have characterized a newly identified 16.6 kb deletion which removes a significant proportion of ...
In alpha-thalassemia, the genetic locus for the alpha chains of adult hemoglobin is not expressed. W...
Genetic variation at the human a-globin gene complex has only been characterised to date ...
In alpha-thalassemia, the genetic locus for the alpha chains of adult hemoglobin is not expressed. W...
Most cases of {alpha}-thalassemia result from large deletions at the {alpha}-globin locus (1). The {...
Alpha-thalassemia is an inherited hemoglobin disorder characterized by a microcytic hypochromic anem...