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Hemoglobin, ISSN 0363-0269, 05/2019, Volume 43, Issue 3, pp. 162 - 165
In Bangladesh, the practice of β-thalassemia (β-thal) carrier screening and prenatal diagnosis (PND) by β-globin gene sequencing has been initiated to prevent... 
β-Thalassemia (β-thal) | sequencing analysis | novel de novo mutation
Journal Article
Hemoglobin, ISSN 0363-0269, 05/2019, Volume 43, Issue 3, pp. 155 - 161
β-Thalassemia (β-thal), is an inherited blood disorder caused by reduced or absent synthesis of β-globin chains leading to imbalance of globin chain synthesis.... 
anemia severity | phagocytosis | β-thalassemia (β-thal) | microRNA-125b (miR-125b) | Activated monocyte
Journal Article
Hemoglobin, ISSN 0363-0269, 05/2019, Volume 43, Issue 3, pp. 198 - 203
β-Thalassemia (β-thal) is a chronic illness and its complications make the patient less compliant with the treatment protocol. This study aimed to evaluate the... 
β-Thalassemia (β-thal) | educational-support | peer group | self-care
Journal Article
Hemoglobin, ISSN 0363-0269, 05/2019, Volume 43, Issue 3, pp. 174 - 181
β-Thalassemia (β-thal) is the most common hereditary genetic blood disorder. The aims of this study were: (i) to determine the mutation types and the frequency... 
in silico analysis | mutation | Ethnicity | β-thalassemia (β-thal) | hemoglobin (Hb) disorders
Journal Article
Hemoglobin, ISSN 0363-0269, 05/2019, Volume 43, Issue 3, pp. 218 - 221
Hypothyroidism is one of the common endocrine complications described in patients with β-thalassemia major (β-TM). Studies have reported its incidence and... 
β-Thalassemia (β-thal) | deferoxamine (DFO) | ferritin | thyroid | Syria
Journal Article
Hemoglobin, ISSN 0363-0269, 07/2018, Volume 42, Issue 4, pp. 272 - 275
β-Thalassemia (β-thal) is one of the most common autosomal recessive disorders worldwide. It is caused mainly by point mutations or, more rarely, deletions on... 
multiplex ligation-dependent probe amplification (MLPA) | β-Globin gene | β-thalassemia (β-thal) | deletion
Journal Article
Annals of Hematology, ISSN 0939-5555, 07/2009, Volume 89, Issue 2, pp. 127 - 134
The study of the alleles of the δ-globin gene is relevant to the prevention of β-thalassemia homozygosis; in fact, the increase of the HbA2 is an invaluable... 
Journal Article
Hemoglobin, ISSN 0363-0269, 05/2018, Volume 42, Issue 3, pp. 143 - 147
The aim of this study was to explore the type and distribution of α- and β-thalassemia (α- and β-thal) mutations/deletions in Fuzhou, Fujian Province, People's... 
α-Thalassemia (α-thal) | β-thalassemia (β-thal) | gene mutation type
Journal Article
Hemoglobin, ISSN 0363-0269, 03/2018, Volume 42, Issue 2, pp. 135 - 137
A Chinese family with δ-thalassemia (δ-thal) was found, in which the daughter is homozygous for δ-thal (HBD: c.-127T>C) with complete deficiency of Hb A 2 and... 
β-Thalassemia (β-thal) | δ-thalassemia (δ-thal) | mutation detection | HBD gene
Journal Article
Hemoglobin, ISSN 0363-0269, 05/2018, Volume 42, Issue 3, pp. 189 - 193
The prevalence of atrial fibrillation (AFib) in β-thalassemia major (β-TM) patients has increased in the last few years, reaching up to 33.0%. Several factors... 
atrial fibrillation (AFib) | iron overload | β-thalassemia (β-thal) | Arrhythmia
Journal Article
Hemoglobin, ISSN 0363-0269, 11/2015, Volume 39, Issue 6, pp. 445 - 447
β-Thalassemia (β-thal) is the most widespread autosomal recessive disorder worldwide. The present study describes a very rare β-globin gene mutation, codon 54... 
β-Thalassemia (β-thal) | Iran | HBB: c.165delT mutation
Journal Article
Hemoglobin, ISSN 0363-0269, 01/2016, Volume 40, Issue 1, pp. 25 - 28
Journal Article
Hemoglobin, ISSN 0363-0269, 11/2017, Volume 41, Issue 4-6, pp. 291 - 292
Coinheritance of δ-globin variants along with β-globin gene defects can interfere with correct diagnosis of β-thalassemia (β-thal) trait. In this report, we... 
β-Thalassemia (β-thal) | Hb A | Tianhe | δ chain hemoglobin (Hb) variant
Journal Article
Hemoglobin, ISSN 0363-0269, 01/2019, Volume 43, Issue 1, pp. 18 - 22
β-Thalassemia (β-thal) is one of the most common hemoglobinopathies worldwide and is caused by mutations on the β-globin (HBB) gene. The aim of the present... 
β-Thalassemia (β-thal) | Mutation | Iran | gene | beta-Thalassemia (beta-thal) | BIOCHEMISTRY & MOLECULAR BIOLOGY | HEMATOLOGY | MOLECULAR-SPECTRUM
Journal Article
Hemoglobin, ISSN 0363-0269, 05/2017, Volume 41, Issue 3, pp. 193 - 197
β-Thalassemia (β-thal) is the most common inherited hemolytic anemia worldwide. Elevated Hb A 2 is a mark of β-thal carriers. The aim of this study was to... 
β-Thalassemia (β-thal) | Hb A | rs231841 polymorphism | positive natural selection
Journal Article
BMC Pediatrics, ISSN 1471-2431, 02/2019, Volume 19, Issue 1, pp. 61 - 5
Beta thalassemia (β-thal) is an inherited hemoglobin disorder characterized by reduced synthesis of the hemoglobin that results in microcytic hypochromic... 
Hb Knossos | β-Thalassemia (β-thal) | Mutations | Syria | δ-Thalassemia (δ-thal) | Blood transfusions | Genotype & phenotype | Hematology | Anemia | Hemoglobin | Mutation | Blood | Polymorphism
Journal Article
Hemoglobin, ISSN 0363-0269, 05/2018, Volume 42, Issue 3, pp. 154 - 158
Increased Hb A 2 is considered the most reliable hematological finding for the identification of β-thalassemia (β-thal) carriers. The aim of this study was to... 
Hb A | screening | β-thalassemia (β-thal) | Krüppel-like factor 1 (KLF1) gene mutations | α-Thalassemia (α-thal)
Journal Article
Cogent Medicine, ISSN 2331-205X, 01/2019, Volume 6, Issue 1
Beta-thalassemia (β-thal) is an inherited hemoglobin disorder, characterized by the absence of or reduced hemoglobin chains that result in microcytic... 
β-Thalassemia (β-thal) | rare mutations | 29 A>G beta | thalassemia intermedia | Syria
Journal Article
Cogent Medicine, 02/2019
Beta thalassemia (β-thal) is an inherited hemoglobin disorder, it characterized by absence or reduced of the hemoglobin chains that results in microcytic... 
β-Thalassemia (β-thal) | Rare mutations | 29 A>G beta+ | thalassemia intermedia | Syria
Journal Article
Hemoglobin, ISSN 0363-0269, 01/2017, Volume 41, Issue 1, pp. 47 - 49
We first report a novel β chain variant, Hb Heze [β144(HC1)Lys→Arg; HBB: c.434A>G], in a Chinese family. Heterozygous inheritance of the mutation results in a... 
β-Chain variant | hemoglobin (Hb) variant | β-thalassemia (β-thal)
Journal Article
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