Essential genetic modifiers and their measurable impact in a community-recruited population analysis for non-severe hemoglobin E/β-thalassemia prenatal genetic counseling

Genetic polymorphisms of HbE/beta thalassemia related to clinical presentation: implications for clinical diversity

(2020) Nurul Fatihah Azman et al.   ANNALS OF HEMATOLOGY

A novel mutation in the erythroid transcription factor KLF1 is likely responsible for ameliorating β‐thalassemia major

(2019) Pavlos Fanis et al.   HUMAN MUTATION

Genetic variation of Krüppel-like factor 1 (KLF1) and fetal hemoglobin (HbF) levels in β0-thalassemia/HbE disease

(2017) Pinyaphat Khamphikham et al.   INTERNATIONAL JOURNAL OF HEMATOLOGY

A genetic score for the prediction of beta-thalassemia severity

(2014) F. Danjou et al.   HAEMATOLOGICA

A Single Nucleotide Polymorphism in theHBBP1Gene in the Human β-Globin Locus is Associated with a Mild β-Thalassemia Disease Phenotype

(2012) Emily Giannopoulou et al.   HEMOGLOBIN

HbE/β-Thalassemia: Basis of Marked Clinical Diversity

(2010) Nancy F. Olivieri et al.   HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA

A scoring system for the classification of β-thalassemia/Hb E disease severity

(2008) Orapan Sripichai et al.   AMERICAN JOURNAL OF HEMATOLOGY

Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-β-thalassemia in Northeast Thailand

(2008) L NUNTAKARN et al.   BLOOD CELLS MOLECULES AND DISEASES

Global epidemiology of haemoglobin disorders and derived service indicators

(2008) Bernadette Modell   BULLETIN OF THE WORLD HEALTH ORGANIZATION