Mutation patterns in the HBB gene determine the frequency and onset of blood transfusion in patients with beta-thalassemia major and HbE-beta thalassemia
This thesis report is submitted in partial fulfilment of the requirement for the degree of Master of Science in Biotechnology, 2019.
Prif Awdur: | Tasnim, Raisa |
---|---|
Awduron Eraill: | Hossain, Mahboob |
Fformat: | Traethawd Ymchwil |
Iaith: | English |
Cyhoeddwyd: |
Brac University
2020
|
Pynciau: | |
Mynediad Ar-lein: | http://hdl.handle.net/10361/13806 |
Eitemau Tebyg
-
Study on the frequency of single nucleotide polymorphism (rs766432) in BCL11A gene and its association with hematological parameter and HbF level among HbE/β -thalassemia patients in Bangladeshi population
gan: Barno, Shadman Sakib
Cyhoeddwyd: (2022) -
Hematological analysis of anemic severity in beta thalassemia
gan: Barno, Shadman Sakib
Cyhoeddwyd: (2018) -
Detection of beta globin gene mutations in thalassemia patients in Bangladesh and correlation with hematological parameters
gan: Biswas, Aparna
Cyhoeddwyd: (2019) -
Comparison of mutation spectrum, hemoglobin profiles and hematological features between transfusion dependent and non-dependent patients of Hb E/β Thalassemia
gan: Islam, Maliha
Cyhoeddwyd: (2020) -
Knowledge, Attitude and Practice (KAP) study for thalassemia: a cross-sectional study at BRAC University, Bangladesh
gan: Mim, Afsana
Cyhoeddwyd: (2023)