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The therapeutic potential of genome editing for β-thalassemiaAnimal models and conserved processesIncreased activity of Diaphanous homolog 3 (DIAPH3)/diaphanous causes hearing defects in humans with auditory neuropathy and in Drosophila.The molecular basis of beta-thalassemia intermedia in southern China: genotypic heterogeneity and phenotypic diversity.A Novel -72 (T→A) β-Promoter Mutation Causing Slightly Elevated HbA2 in a Vietnamese HeterozygoteImpact of genotype on endocrinal complications of Children with Alpha-thalassemia in China.IthaGenes: an interactive database for haemoglobin variations and epidemiologyAmelioration of Sardinian beta0 thalassemia by genetic modifiers.Beta thalassaemia trait in western NigeriaFOXO3-mTOR metabolic cooperation in the regulation of erythroid cell maturation and homeostasis.Combination of two rare mutations causes β-thalassaemia in a Bangladeshi patient.Role of XmnIgG Polymorphism in Hydroxyurea Treatment and Fetal Hemoglobin Level at Isfahanian Intermediate β-Thalassemia Patients.Rapid detection of pathological mutations and deletions of the haemoglobin beta gene (HBB) by High Resolution Melting (HRM) analysis and Gene Ratio Analysis Copy Enumeration PCR (GRACE-PCR)Screening of Transcription Factors Involved in Fetal Hemoglobin Regulation Using Phylogenetic Footprinting.Seroprevalence of Hepatitis C, Hepatitis B, Cytomegalovirus, and Human Immunodeficiency Viruses in Multitransfused Thalassemic Children in Upper Egypt.Hemoglobin A2 Lowered by Iron Deficiency and α -Thalassemia: Should Screening Recommendation for β -Thalassemia Change?Evolutionary constraints in the β-globin cluster: the signature of purifying selection at the δ-globin (HBD) locus and its role in developmental gene regulation.Detection of β-globin Gene Mutations Among β-thalassaemia Carriers and Patients in Malaysia: Application of Multiplex Amplification Refractory Mutation System-Polymerase Chain Reaction.Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermedia.Longitudinal study on thyroid function in patients with thalassemia major: High incidence of central hypothyroidism by 18 years.The First Report of a 290-bp Deletion in β-Globin Gene in the South of Iran.Bone microarchitecture deteriorations and a fragility fracture in a patient with beta and alpha heterozygous thalassemia: a case report.Novel Βeta (β)-Thalassemia Mutation in Turkish Children.Identification of patients with defects in the globin genes.Recent advances in β-thalassemiasGenetic epidemiology, hematological and clinical features of hemoglobinopathies in IranBeta-thalassemia: from genotype to phenotype.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Genetic modifiers of beta-thalassemia.
@ast
Genetic modifiers of beta-thalassemia.
@en
type
label
Genetic modifiers of beta-thalassemia.
@ast
Genetic modifiers of beta-thalassemia.
@en
prefLabel
Genetic modifiers of beta-thalassemia.
@ast
Genetic modifiers of beta-thalassemia.
@en
P1433
P1476
Genetic modifiers of beta-thalassemia
@en
P304
P577
2005-05-01T00:00:00Z