We have identified a 16 bp deletion in the 3' untranslated region of the alpha 2-globin gene, including the first nucleotide of the polyadenylation signal sequence. The propositus, her mother and one of her brothers, all heterozygotes for the above deletion, have mild microcytic anemia. This is the first description of a deletion in the alpha gene involving both the 3' untranslated region and the polyadenylation signal sequence, causing alpha-thalassemia
Over 95.0% of the alpha-thalassemia (alpha-thal) cases in southern China are caused by large deletio...
We describe a new deletional form of alpha thalassaemia which encompasses the entire alpha-like glob...
We describe a novel deletion form of alpha-thalassemia which removes a region of 31 kilobase encompa...
We describe a family in which alpha-thalassemia occurs in association with a deletion of 62 kilobase...
The clinical diversity of thalassemia depends on interaction of diverse genetic defects. We have cha...
Item does not contain fulltextAlpha-thalassemia is an inherited hemoglobin disorder characterized by...
Alpha-thalassemia is an inherited hemoglobin disorder characterized by a microcytic hypochromic anem...
We describe a new deletional form of alpha thalassemia segregating in three generations of a family ...
Inherited deletions of α-globin genes and/or their upstream regulatory elements (MCSs) give rise to ...
Most eukaryotic messenger RNAs have the sequence AAUAAA 11-30 nucleotides from the 3'-terminal poly(...
Alpha-thalassemia is the most common inherited disorder of hemoglobin synthesis. Genomic deletions i...
Alpha-thalassemia is the most common inherited disorder of hemoglobin synthesis. Genomic deletions i...
European Society of Human Genetics, 27-30 May 2017Introduction: Inherited deletions removing the α-g...
Most cases of {alpha}-thalassemia result from large deletions at the {alpha}-globin locus (1). The {...
We have identified and characterized a Scottish individual with alpha thalassaemia, resulting from a...
Over 95.0% of the alpha-thalassemia (alpha-thal) cases in southern China are caused by large deletio...
We describe a new deletional form of alpha thalassaemia which encompasses the entire alpha-like glob...
We describe a novel deletion form of alpha-thalassemia which removes a region of 31 kilobase encompa...
We describe a family in which alpha-thalassemia occurs in association with a deletion of 62 kilobase...
The clinical diversity of thalassemia depends on interaction of diverse genetic defects. We have cha...
Item does not contain fulltextAlpha-thalassemia is an inherited hemoglobin disorder characterized by...
Alpha-thalassemia is an inherited hemoglobin disorder characterized by a microcytic hypochromic anem...
We describe a new deletional form of alpha thalassemia segregating in three generations of a family ...
Inherited deletions of α-globin genes and/or their upstream regulatory elements (MCSs) give rise to ...
Most eukaryotic messenger RNAs have the sequence AAUAAA 11-30 nucleotides from the 3'-terminal poly(...
Alpha-thalassemia is the most common inherited disorder of hemoglobin synthesis. Genomic deletions i...
Alpha-thalassemia is the most common inherited disorder of hemoglobin synthesis. Genomic deletions i...
European Society of Human Genetics, 27-30 May 2017Introduction: Inherited deletions removing the α-g...
Most cases of {alpha}-thalassemia result from large deletions at the {alpha}-globin locus (1). The {...
We have identified and characterized a Scottish individual with alpha thalassaemia, resulting from a...
Over 95.0% of the alpha-thalassemia (alpha-thal) cases in southern China are caused by large deletio...
We describe a new deletional form of alpha thalassaemia which encompasses the entire alpha-like glob...
We describe a novel deletion form of alpha-thalassemia which removes a region of 31 kilobase encompa...