Volume 7 (2024)
Volume 6 (2023)
Volume 5 (2022)
Volume 4 (2021)
Volume 3 (2020)
Volume 2 (2019)
Volume 1 (2018)
Keywords = Thalassemia
Number of Articles: 4
Neonatal Sickle Cell Disease Assessment in Rural Indian Community: Demand for Point of Care Testing (POCT)
Volume 7, Issue 1 , January 2024, , Pages 1-8
Abstract
The most prevalent hemoglobinopathy is sickle cell disease, which is followed by β-thalassemia and thalassemia syndrome. The Mediterranean region, Middle East, Indian subcontinent, ... Read MoreHaemoglobin Variant Study by HPLC Method at a Tertiary Care Centre
Volume 6, Issue 11 , November 2023, , Pages 2841-2848
Abstract
Haemoglobinopathies are genetic disorders arising due to defect in the globin chain of haemoglobin. It is relatively common amongst genetic disorders. Beta thalassemia and Sickle cell ... Read MoreAssociation of BCL11A Gene Polymorphism in Human Cells of Thalassemia Patient by Evaluation of Amplification Refractory Mutation System (ARMS)
Volume 6, Issue 4 , April 2023, , Pages 834-845
Abstract
Thalassemia is an autosomal recessive disorder. It occurs due to mutations that lead to a decrease or absence of β-globin chains. In human erythroid cells, it was found that BCL11A ... Read MoreThe Study of BCL11A Gene in Patients with Beta-Thalassemia Major and Intermedia by Random Amplephed Polymorphism DNA in Iraq
Volume 6, Issue 4 , April 2023, , Pages 846-856