Add to ORKGThalassaemia control in India is a complex issue; the financial, social and demographic factors involved were considered and recommendations made
ABSTRACT Aims: Thalassemia is an inherited hemoglobin disorder caused by anomalies in the globin ch...
β Thalassaemia is a major public health problem in India. A comprehensive database of the spect...
Mutation spectrum varies significantly in different parts and different ethnic groups of India. Soci...
SIGLEAvailable from British Library Document Supply Centre- DSC:D98049 / BLDSC - British Library Doc...
BACKGROUND: Thalassaemias pose an increasing problem for the Indian subcontinent and many Asian coun...
guidelines for prenatal diagnosis programmes in the country. Blood samples of patients with beta-tha...
The primary aim of this thesis was to outline an approach for the prenatal diagnosis of β-thalassaem...
There are an estimated 45 million carriers of β-thalassemia trait and about 12,000-15,000 infants wi...
semia mutations in India. ABSTRACT The present study was undertaken with the objective to study mole...
Abstract: Beta-thalassemia is one of the most prevalent autosomal disorders in the world. Mutations ...
In India the incidence of beta thalassemia trait in general population is about 3%. There are a numb...
beta-thalassaemia major, an autosomal recessive hemoglobinopathy, is one of the most common single g...
Beta- Thalassaemia is a group of heterogeneous recessive disorders common in many parts of the world...
As an initial step towards establishing prenatal diagnostic service for beta-thalassaemia in the sta...
Copyright © 2015 Ravindra Kumar et al. This is an open access article distributed under the Creative...
ABSTRACT Aims: Thalassemia is an inherited hemoglobin disorder caused by anomalies in the globin ch...
β Thalassaemia is a major public health problem in India. A comprehensive database of the spect...
Mutation spectrum varies significantly in different parts and different ethnic groups of India. Soci...
SIGLEAvailable from British Library Document Supply Centre- DSC:D98049 / BLDSC - British Library Doc...
BACKGROUND: Thalassaemias pose an increasing problem for the Indian subcontinent and many Asian coun...
guidelines for prenatal diagnosis programmes in the country. Blood samples of patients with beta-tha...
The primary aim of this thesis was to outline an approach for the prenatal diagnosis of β-thalassaem...
There are an estimated 45 million carriers of β-thalassemia trait and about 12,000-15,000 infants wi...
semia mutations in India. ABSTRACT The present study was undertaken with the objective to study mole...
Abstract: Beta-thalassemia is one of the most prevalent autosomal disorders in the world. Mutations ...
In India the incidence of beta thalassemia trait in general population is about 3%. There are a numb...
beta-thalassaemia major, an autosomal recessive hemoglobinopathy, is one of the most common single g...
Beta- Thalassaemia is a group of heterogeneous recessive disorders common in many parts of the world...
As an initial step towards establishing prenatal diagnostic service for beta-thalassaemia in the sta...
Copyright © 2015 Ravindra Kumar et al. This is an open access article distributed under the Creative...
ABSTRACT Aims: Thalassemia is an inherited hemoglobin disorder caused by anomalies in the globin ch...
β Thalassaemia is a major public health problem in India. A comprehensive database of the spect...
Mutation spectrum varies significantly in different parts and different ethnic groups of India. Soci...