[66258_184734=] and heterozygous state of Codon 67 [GTG>ATG] Hb A2-Deventer mutation, NG_000007.3:g.[63512G>A][63512G=] (Figure 1 and 2). Detection of 5 unrelated cases of HbA2 Deventer may suggest that this delta variant is common among indigenous Sabahan. Since beta thalassaemia is also common in the population, more attention should be paid during diagnosis. Identification of delta variant in beta thalassaemia carrier is important because coinheritance of beta and delta thalassaemia results in a less elevated HbA2 level. Therefore, molecular testing of thalassemia carrier state in the case of borderline HbA2 is warranted to avoid misdiagnosis of beta thalassaemia carriers
beta- thalassemia is the most-common genetic disorder of hemoglobin synthesis in Malaysia, and about...
A 42-year-old Chinese woman (FP) was the mother of a patient with β-thalassemia major (β-TM) due to ...
Interpreting hemoglobin disorders by high performance liquid chromatography can sometimes deceptive,...
Introduction: HbE is the commonest beta haemoglobin (Hb) variant in Southeast Asia. It causes a re...
Introduction: HbE is the commonest beta haemoglobin (Hb) variant in Southeast Asia. It causes a redu...
Beta thalassaemia is one of the most common inherited haemoglobinopathies, characterised by reduced ...
HbA2' is a haematologically silent delta chain variant that elutes in the S-region on high performan...
Beta-thalassemia is one of the most prevalent inherited diseases and a public health problem in Mala...
Level of HbA2 more than 4% is the reliable parameter to identify β- thalassemia carrier. However, in...
Background/Aims: Individuals with double heterozygosity for alpha- and beta-thalassaemia and heteroz...
Level of HbA2 more than 4% is the reliable parameter to identify β- thalassemia carrier. However, in...
This finding confirmed the deletion in the homozygous state was associated with a severe phenotype. ...
Sabah has the largest number of β-thalassaemia major (β-TM) patients in Malaysia with estimated over...
We report a novel thalassemia determinant found in a Nigerian woman living in the Netherlands, resul...
Co-inheritance of alpha-thalassemia with homozygosity or compound heterozygosity for beta-thalassemi...
beta- thalassemia is the most-common genetic disorder of hemoglobin synthesis in Malaysia, and about...
A 42-year-old Chinese woman (FP) was the mother of a patient with β-thalassemia major (β-TM) due to ...
Interpreting hemoglobin disorders by high performance liquid chromatography can sometimes deceptive,...
Introduction: HbE is the commonest beta haemoglobin (Hb) variant in Southeast Asia. It causes a re...
Introduction: HbE is the commonest beta haemoglobin (Hb) variant in Southeast Asia. It causes a redu...
Beta thalassaemia is one of the most common inherited haemoglobinopathies, characterised by reduced ...
HbA2' is a haematologically silent delta chain variant that elutes in the S-region on high performan...
Beta-thalassemia is one of the most prevalent inherited diseases and a public health problem in Mala...
Level of HbA2 more than 4% is the reliable parameter to identify β- thalassemia carrier. However, in...
Background/Aims: Individuals with double heterozygosity for alpha- and beta-thalassaemia and heteroz...
Level of HbA2 more than 4% is the reliable parameter to identify β- thalassemia carrier. However, in...
This finding confirmed the deletion in the homozygous state was associated with a severe phenotype. ...
Sabah has the largest number of β-thalassaemia major (β-TM) patients in Malaysia with estimated over...
We report a novel thalassemia determinant found in a Nigerian woman living in the Netherlands, resul...
Co-inheritance of alpha-thalassemia with homozygosity or compound heterozygosity for beta-thalassemi...
beta- thalassemia is the most-common genetic disorder of hemoglobin synthesis in Malaysia, and about...
A 42-year-old Chinese woman (FP) was the mother of a patient with β-thalassemia major (β-TM) due to ...
Interpreting hemoglobin disorders by high performance liquid chromatography can sometimes deceptive,...