We describe a new deletional form of gamma delta beta-thalassemia segregating in two generations of a family of Irish descent. Affected family members present with a beta-thalassemia minor phenotype, normal Hb A2 and Hb F levels. Genomic blotting analyses on DNA from affected family members show heterozygosity for a large deletion beginning at least 15 kb upstream of the 5' endpoint of the gamma delta beta-thalassemia-1 deletion, extending through the entire beta-like globin gene cluster, and continuing for at least 10 kb beyond the 3' endpoint of the deletion associated with the Spanish form of delta beta 0-thalassemia. This deletion is among the largest described so far, and removes at least 205 kb encompassing the entire beta-like globin...
Large deletions of the beta-globin gene cluster are problematic to diagnose, and consequently the fr...
European Society of Human Genetics, 27-30 May 2017Introduction: Inherited deletions removing the α-g...
A family was studied in which two inherited defects of the non-alpha-globin cluster segregate: Greek...
textabstractWe have used restriction endonuclease mapping to study a deletion involving the beta-glo...
We describe a new deletional form of alpha thalassemia segregating in three generations of a family ...
Spanish \u3b4\u3b2\ub0-thalassemia, a mild thalassemic condition characterized by increased level of...
We describe a new deletional form of alpha thalassaemia which encompasses the entire alpha-like glob...
We describe a novel deletion causing heterozygous εγδβ-thalassemia (εγδβ-thal) across three generati...
textabstractThe DNA spanning two large deletions in the human beta-globin gene cluster (gamma beta-t...
Alpha-thalassemia is an inherited hemoglobin disorder characterized by a microcytic hypochromic anem...
We describe a family carrying a g-globin gene deletion associated with an increase of Hb A2 level b...
Alpha-thalassemia is an inherited hemoglobin disorder characterized by a microcytic hypochromic anem...
The major component of the red blood cells is hemoglobin A which consists of 2α- and 2β-globin chain...
Thalassemia is among the most common genetic diseases worldwide. α-Thalassemia is usually caused by ...
The analysis of a number of cases of beta-globin thalassemia and hereditary persistence of...
Large deletions of the beta-globin gene cluster are problematic to diagnose, and consequently the fr...
European Society of Human Genetics, 27-30 May 2017Introduction: Inherited deletions removing the α-g...
A family was studied in which two inherited defects of the non-alpha-globin cluster segregate: Greek...
textabstractWe have used restriction endonuclease mapping to study a deletion involving the beta-glo...
We describe a new deletional form of alpha thalassemia segregating in three generations of a family ...
Spanish \u3b4\u3b2\ub0-thalassemia, a mild thalassemic condition characterized by increased level of...
We describe a new deletional form of alpha thalassaemia which encompasses the entire alpha-like glob...
We describe a novel deletion causing heterozygous εγδβ-thalassemia (εγδβ-thal) across three generati...
textabstractThe DNA spanning two large deletions in the human beta-globin gene cluster (gamma beta-t...
Alpha-thalassemia is an inherited hemoglobin disorder characterized by a microcytic hypochromic anem...
We describe a family carrying a g-globin gene deletion associated with an increase of Hb A2 level b...
Alpha-thalassemia is an inherited hemoglobin disorder characterized by a microcytic hypochromic anem...
The major component of the red blood cells is hemoglobin A which consists of 2α- and 2β-globin chain...
Thalassemia is among the most common genetic diseases worldwide. α-Thalassemia is usually caused by ...
The analysis of a number of cases of beta-globin thalassemia and hereditary persistence of...
Large deletions of the beta-globin gene cluster are problematic to diagnose, and consequently the fr...
European Society of Human Genetics, 27-30 May 2017Introduction: Inherited deletions removing the α-g...
A family was studied in which two inherited defects of the non-alpha-globin cluster segregate: Greek...