Thailand deletion of alpha-Thalassemia (thal) 1 involves the zeta 2-, phi zeta 1-, alpha 2-, alpha 1-, and 01-globin genes. In Southeast Asians and Taiwanese, this mutation is the second most common long-segment deletion of two alpha- globin genes, after the Southeast Asian deletion, To define the Thailand deletion breakpoints, we used polymerase chain reaction (PCR) to amplify the normal-sequence DNA fragments across the breakpoints. The amplified products were sequenced directly or after cloning into pGem(R)-3 Z or pCR(R )2.1 vectors, Com parison of the normal and mutant sequences revealed that the 5' breakpoint lies between nucleotides 1, 269 and 1,290 upstream of the initiator codon adenine of the zeta 2-globin gene, and the 3' breakpoi...
?-Thalassemia is one of the most prevalent hemoglobin disorders in the world, in South-East Asians, ...
Over 95.0% of the alpha-thalassemia (alpha-thal) cases in southern China are caused by large deletio...
Objectives: This study was designed to delineate the molecular lesions, on DNA level, that lead to α...
We applied PCR strategies to detect the common types of ホア- thalassemia determinants which were asso...
a-Thalassemia is one of the most serious genetically transmitted diseases creating health problems i...
Background: Conventional diagnostic strategy for thalassemia carriers is time-consuming and requires...
Background: Deletions in the f-globin cluster causing thalassaemia and hereditary persistence of fe...
Abstract β-thalassemia is a syndrome characterized by a reduction or complete absence of the β-globi...
α-thalassemia is characterized in about 80% of cases by deletions generated by the presence of dupli...
Most cases of {alpha}-thalassemia result from large deletions at the {alpha}-globin locus (1). The {...
Spring (Hb CS), caused by a termination codon mutation (TAA→CAA) in the α2 gene, is the most common ...
Introduction: Alpha thalassaemia is a highly prevalent disease globally and is a well-known public h...
BACKGROUND AND OBJECTIVES: Hemoglobin Constant Spring (Hb CS), caused by a termination codon mutatio...
Alpha (?) thalassaemia is the most common inherited disorder in Malaysia. The clinical severity is d...
Background: The interaction of the non-deletional α+thalassaemia mutations Haemoglobin Constant Spri...
?-Thalassemia is one of the most prevalent hemoglobin disorders in the world, in South-East Asians, ...
Over 95.0% of the alpha-thalassemia (alpha-thal) cases in southern China are caused by large deletio...
Objectives: This study was designed to delineate the molecular lesions, on DNA level, that lead to α...
We applied PCR strategies to detect the common types of ホア- thalassemia determinants which were asso...
a-Thalassemia is one of the most serious genetically transmitted diseases creating health problems i...
Background: Conventional diagnostic strategy for thalassemia carriers is time-consuming and requires...
Background: Deletions in the f-globin cluster causing thalassaemia and hereditary persistence of fe...
Abstract β-thalassemia is a syndrome characterized by a reduction or complete absence of the β-globi...
α-thalassemia is characterized in about 80% of cases by deletions generated by the presence of dupli...
Most cases of {alpha}-thalassemia result from large deletions at the {alpha}-globin locus (1). The {...
Spring (Hb CS), caused by a termination codon mutation (TAA→CAA) in the α2 gene, is the most common ...
Introduction: Alpha thalassaemia is a highly prevalent disease globally and is a well-known public h...
BACKGROUND AND OBJECTIVES: Hemoglobin Constant Spring (Hb CS), caused by a termination codon mutatio...
Alpha (?) thalassaemia is the most common inherited disorder in Malaysia. The clinical severity is d...
Background: The interaction of the non-deletional α+thalassaemia mutations Haemoglobin Constant Spri...
?-Thalassemia is one of the most prevalent hemoglobin disorders in the world, in South-East Asians, ...
Over 95.0% of the alpha-thalassemia (alpha-thal) cases in southern China are caused by large deletio...
Objectives: This study was designed to delineate the molecular lesions, on DNA level, that lead to α...