Detection of beta globin gene mutations in thalassemia patients in Bangladesh and correlation with hematological parameters
This thesis report is submitted in partial fulfilment of the requirement for the degree of Master of Science in Biotechnology, 2018.
Hlavní autor: | Biswas, Aparna |
---|---|
Další autoři: | Mannoor, Md. Kaiissar |
Médium: | Diplomová práce |
Jazyk: | English |
Vydáno: |
Brac University
2019
|
Témata: | |
On-line přístup: | http://hdl.handle.net/10361/12390 |
Podobné jednotky
-
Mutation patterns in the HBB gene determine the frequency and onset of blood transfusion in patients with beta-thalassemia major and HbE-beta thalassemia
Autor: Tasnim, Raisa
Vydáno: (2020) -
Comparison of mutation spectrum, hemoglobin profiles and hematological features between transfusion dependent and non-dependent patients of Hb E/β Thalassemia
Autor: Islam, Maliha
Vydáno: (2020) -
Hematological analysis of anemic severity in beta thalassemia
Autor: Barno, Shadman Sakib
Vydáno: (2018) -
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
Autor: Barno, Shadman Sakib
Vydáno: (2022) -
Knowledge, Attitude and Practice (KAP) study for thalassemia: a cross-sectional study at BRAC University, Bangladesh
Autor: Mim, Afsana
Vydáno: (2023)