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Annals of Hematology, ISSN 0939-5555, 2/2019, Volume 98, Issue 2, pp. 289 - 299
Thalassaemia are the most common inherited autosomal recessive single gene disorders characterized by chronic hereditary haemolytic anaemia due to the absence... 
Alpha-deletion | Foetal haemoglobin (HbF) | Transfusion | Medicine & Public Health | Hematology | Xmn1 polymorphism | Oncology | Hydroxyurea | HbE-β thalassaemia
Journal Article
ANNALS OF HEMATOLOGY, ISSN 0939-5555, 02/2019, Volume 98, Issue 2, pp. 289 - 299
Thalassaemia are the most common inherited autosomal recessive single gene disorders characterized by chronic hereditary haemolytic anaemia due to the absence... 
REQUIREMENTS | Transfusion | BCL11A | Xmn1 polymorphism | HbE- thalassaemia | Hydroxyurea | HBS1L-MYB | DISORDERS | INTERMEDIA | Alpha-deletion | Foetal haemoglobin (HbF) | POLYMORPHISMS | HYDROXYUREA THERAPY | EXPERIENCE | BETA-THALASSEMIA | HEMATOLOGY | DELETIONS
Journal Article
Journal of Genetics, ISSN 0022-1333, 06/2018, Volume 97, Issue 2, pp. 505 - 511
Journal Article
Cogent Medicine, ISSN 2331-205X, 01/2019, Volume 6, Issue 1
Fetal hemoglobin (HbF) is an essential modifier of sickle cell disease (SCD). The main medical treatment for SCD depends on the induction of HbF by... 
consanguineous marriage | fetal hemoglobin | hydroxyurea | Xmn1 polymorphism | sickle cell disease
Journal Article
Journal of Magnetism and Magnetic Materials, ISSN 0304-8853, 03/2015, Volume 377, pp. 40 - 43
The electronic structure, magnetism and phase stability of Pt Mn Ga ( =0, 0.25, 0.5, 0.75, 1) alloys are studied by first-principle calculations. The... 
Heusler alloys | First-principles calculations | Magnetic martensitic transformation | Pt2−xMn1+xGa | Pt2-xMn1+xGa | PSEUDOPOTENTIALS | PHYSICS, CONDENSED MATTER | CASTEP | MATERIALS SCIENCE, MULTIDISCIPLINARY | MARTENSITIC-TRANSFORMATION
Journal Article
PEDIATRIC BLOOD & CANCER, ISSN 1545-5009, 12/2011, Volume 57, Issue 6, pp. 1025 - 1028
Background. To determine the prevalence of Xmn1-(G)gamma polymorphism in North Indian children and adolescents with beta thalassemia intermedia (TI) and to... 
phenotype | Xmn1-(G)gamma polymorphism | ONCOLOGY | thalassemia syndromes | PEDIATRICS | HEMATOLOGY | MOLECULAR-BASIS | INDIANS | Asian Indians | genotype
Journal Article
MOLECULAR BIOLOGY REPORTS, ISSN 0301-4851, 05/2014, Volume 41, Issue 5, pp. 3331 - 3337
Haemoglobinopathies including beta-thalassemia and sickle cell anaemia (SCA) are considered to be classical monogenic diseases. There is considerable clinical... 
FETAL-HEMOGLOBIN LEVELS | Clinical severity | GENE | BCL11A | Xmn1 polymorphism | BIOCHEMISTRY & MOLECULAR BIOLOGY | beta-Thalassemia | HBS1L-MYB | Modifier genes | Sickle cell anaemia | EXPRESSION
Journal Article
International Journal of Hematology-Oncology and Stem Cell Research, ISSN 1735-1243, 2015, Volume 9, Issue 4, pp. 198 - 202
Thalassemia syndromes are the most prevalent single gene disorders in Iran. This study aimed to evaluate the effect of different types of beta-globin gene... 
α-thalassemia | Iran | β-thalassemia intermedia | β-thalassemia major | Xmn1 polymorphism | Original
Journal Article
JOURNAL OF GENETICS, ISSN 0022-1333, 06/2018, Volume 97, Issue 2, pp. 505 - 511
Journal Article
Pediatric Blood and Cancer, ISSN 1545-5009, 12/2011, Volume 57, Issue 6, pp. 1025 - 1028
Journal Article
Molecular Biology Reports, ISSN 0301-4851, 1/2010, Volume 37, Issue 1, pp. 159 - 164
β-Thalassemia is the most common single gene disorder in Iran and more than 25,000 affected individuals have been reported. It has been reported that in... 
Life Sciences | Splenectomy | Age at first blood transfusion | Animal Biochemistry | Thalassemia | Xmn1 polymorphic site | Facial bone deformity | Animal Anatomy / Morphology / Histology | G γ chain percent | γ chain percent
Journal Article
by Donaldson and Old and Fisher and Serjeant
British Journal of Haematology, ISSN 0007-1048, 02/2000, Volume 108, Issue 2, pp. 290 - 294
The sickling disorders are a common cause of morbidity and mortality in Jamaica. Sickle cell β+-thalassaemia is the fourth commonest form, occurring in one in... 
Xmn1 | amplification refractory mutation system (ARMS) polymerase chain reaction (PCR) | haematology | Jamaica | Sβ+-thalassaemia
Journal Article
British Journal of Haematology, ISSN 0007-1048, 2000, Volume 108, Issue 2, pp. 290 - 294
Journal Article
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