Characterization of New Alpha Zero (α0) Thalassaemia Deletion (−−GB) among Malays in Malaysian Population
NM Yasin, FS Abdul Hamid, S Hassan, Y Mat Yusoff… - Diagnostics, 2023 - mdpi.com
Malaysia is a multicultural and multiethnic country comprising numerous ethnic groups.
From the total population of 32.7 million, Malays form the bulk of the Bumiputera in Malaysia …
From the total population of 32.7 million, Malays form the bulk of the Bumiputera in Malaysia …
Frequency Of Beta Thalassemia Major Abo Blood Groups In Different Foundation Of District Peshawar
Background: Thalassemia major (TM) is an inherited hemolytic disorder occur due to
abnormal hemoglobin production as a result of HBB (Haemoglobin Subunit Beta) gene …
abnormal hemoglobin production as a result of HBB (Haemoglobin Subunit Beta) gene …
THALASSEMIA: MOLECULAR GENETIC DIAGNOSTIC METHODS
LA Mirzoeva, GN Davlatova, KT Boboev - … Multidisciplinary Journal for …, 2023 - ijmrd.in
INTERNATIONAL MULTIDISCIPLINARY JOURNAL FOR RESEARCH & DEVELOPMENT SJIF
2019: 5.222 2020: 5.552 2021: 5.637 2022:5.479 2023: Page 1 INTERNATIONAL …
2019: 5.222 2020: 5.552 2021: 5.637 2022:5.479 2023: Page 1 INTERNATIONAL …
Alpha thalassemia in Istanbul: Distribution of deletions in alpha-globin gene cluster
FN Öztürk - Genel Tıp Dergisi - dergipark.org.tr
Amaç: Alfa talasemi, alfa globin gen kümesindeki genler tarafından kodlanan bir globin
protein bozukluğu nedeniyle ortaya çıkan otozomal resesif kalıtsal bir hastalıktır. Hafif …
protein bozukluğu nedeniyle ortaya çıkan otozomal resesif kalıtsal bir hastalıktır. Hafif …