The triplicated alpha gene locus has been described independently by Higgs et a1 (1980) and Goossems et aI (1 980). The coinheritance of heterozygous beta-thalassaemia and the additional alpha gene has been recently reported by Kanavakis et aZ(1983). They observed that, in subjects of Greek and Indian origin, the interaction of the two genetic abnormalities is haematologically and clinically indistinguishable from heterozygous beta-thalassaemia. In this paper, we report a case in which the same interaction seems to give rise to a picture of mild thalassaemia intermedia
The –α 3.7 rightward deletion is the most frequent α-globin mutation but ααα (anti 3.7) triplication...
Alpha-thalassaemia is inherited as an autosomal recessive disorder characterised by a microcytic hyp...
The clinical diversity of thalassemia depends on interaction of diverse genetic defects. We have cha...
The triplicated alpha gene locus has been described independently by Higgs et a1 (1980) and Goossems...
We report a case in which the interaction of heterozygosis for both the beta(0)-IVS-II-1 (G-->A) mut...
The pathophysiology and clinical severity of beta-thalassemia are related to the degree of alpha/non...
The presence of extra copies of alpha-globin gene has been shown to worsen the degree of anemia in b...
We describe a case in which the interaction of heterozygosis for the mutation Beta IVSI - 110 G> A a...
We describe two cases of simple heterozygosity for the common β°-thalassemia mutation β39 (C → T), b...
Background/Aims: Individuals with double heterozygosity for alpha- and beta-thalassaemia and heteroz...
We report a case in which the interaction of heterozygosis for both the ß0-IVS-II-1 (G->A) mutation ...
Co-inheritance of alpha-thalassemia with homozygosity or compound heterozygosity for beta-thalassemi...
The association of alfa-gene quadruplication and heterozygous beta-thalassemia has been recognized i...
This paper reports a Sardinian patient, who was a compound heterozygote for silent beta-thalassaemia...
In this study, we analyzed the phenotypic manifestations resulting from the interaction of heterozyg...
The –α 3.7 rightward deletion is the most frequent α-globin mutation but ααα (anti 3.7) triplication...
Alpha-thalassaemia is inherited as an autosomal recessive disorder characterised by a microcytic hyp...
The clinical diversity of thalassemia depends on interaction of diverse genetic defects. We have cha...
The triplicated alpha gene locus has been described independently by Higgs et a1 (1980) and Goossems...
We report a case in which the interaction of heterozygosis for both the beta(0)-IVS-II-1 (G-->A) mut...
The pathophysiology and clinical severity of beta-thalassemia are related to the degree of alpha/non...
The presence of extra copies of alpha-globin gene has been shown to worsen the degree of anemia in b...
We describe a case in which the interaction of heterozygosis for the mutation Beta IVSI - 110 G> A a...
We describe two cases of simple heterozygosity for the common β°-thalassemia mutation β39 (C → T), b...
Background/Aims: Individuals with double heterozygosity for alpha- and beta-thalassaemia and heteroz...
We report a case in which the interaction of heterozygosis for both the ß0-IVS-II-1 (G->A) mutation ...
Co-inheritance of alpha-thalassemia with homozygosity or compound heterozygosity for beta-thalassemi...
The association of alfa-gene quadruplication and heterozygous beta-thalassemia has been recognized i...
This paper reports a Sardinian patient, who was a compound heterozygote for silent beta-thalassaemia...
In this study, we analyzed the phenotypic manifestations resulting from the interaction of heterozyg...
The –α 3.7 rightward deletion is the most frequent α-globin mutation but ααα (anti 3.7) triplication...
Alpha-thalassaemia is inherited as an autosomal recessive disorder characterised by a microcytic hyp...
The clinical diversity of thalassemia depends on interaction of diverse genetic defects. We have cha...