Molecular basis of a high Hb A2/Hb Fβ-thalassemia trait: a retrospective analysis, genotype-phenotype interaction, diagnostic implication, and identification of a novel …
Background β 0-thalassemia deletion removing 5 β-globin promoter usually presents
phenotype with high hemoglobin (Hb) A 2 and Hb F levels. We report the molecular …
phenotype with high hemoglobin (Hb) A 2 and Hb F levels. We report the molecular …
First Report of Filipino β0-Thalassemia/β-Thalassemia in a Chinese Family
M Chen, A Lv, S Zhang, J Zheng, M Zhang, L Chen… - …, 2024 - Taylor & Francis
A pregnant woman living in Fujian Province, southeastern China, presented due to a risk of
having a baby with β-thalassemia major, during her second pregnancy, since she and her …
having a baby with β-thalassemia major, during her second pregnancy, since she and her …
Genotype-phenotype study of β-thalassemia patients in Sabah
Abstract β-thalassemia is a serious public health problem in Sabah due to its high
prevalence. This study aimed to investigate the effects of different types of β-globin gene …
prevalence. This study aimed to investigate the effects of different types of β-globin gene …
The Effect of Single Nucleotide Polymorphisms on Clinical Phenotypes of Sabahan Transfusion-Dependent β-Thalassemia Patients with Homozygous Filipino β0 …
Sabah has the highest prevalence of β-thalassemia in Malaysia, with the Filipino β0-deletion
as the predominant mutation. Patients with the homozygous Filipino β0-deletion exhibit …
as the predominant mutation. Patients with the homozygous Filipino β0-deletion exhibit …
[PDF][PDF] Demographic and Socioeconomic Profile of Transfusion Dependent Beta-Thalassemia Major Patients in Sabah.
ABSTRACT Introduction: Thalassemia prevalence in Malaysia is highest in Sabah. This
study was conducted to characterize the demographic and socioeconomic profile of …
study was conducted to characterize the demographic and socioeconomic profile of …
Prevalence of RDB, RSa, Hinc and Xmn polymorphisms and HBBS11D haplotypes in patients with thalassemia minor
SS Irankhah, S Hoseini-Asl, M Valizadeh… - Cellular, Molecular …, 2022 - cmbr-journal.com
Background: Beta-thalassemia is one of the most common genetic diseases with autosomal
recessive inherited patterns in the world and is one of the most common diseases in Iran that …
recessive inherited patterns in the world and is one of the most common diseases in Iran that …
[PDF][PDF] To Study the β-Globin Haplotype Pattern of Descent of a Set of Linked Alleles Occurring on the Same Chromosome in the Northern Province of India
Objective: To study the five mutations commonly prevalent in North India, ie, IVS-I-5 (G→ C),
619 bp deletion, IVS-I-1 (G→ T), codon 41/42 (-TTCT), and codon 8/9 (+ G), in the beta …
619 bp deletion, IVS-I-1 (G→ T), codon 41/42 (-TTCT), and codon 8/9 (+ G), in the beta …
MOTHERS WITH MULTIPLE β-THALASSEMIA MAJOR CHILDREN IN SABAH, MALAYSIA: A QUALITATIVE STUDY EXPLORING THE CONTRIBUTING FACTORS …
Despite having the highest prevalence of thalassemia in Malaysia, studies exploring factors
that contribute to high thalassemia births in Sabah is still lacking. This study aimed to …
that contribute to high thalassemia births in Sabah is still lacking. This study aimed to …