A Novel -72 (T→A) β-Promoter Mutation Causing Slightly Elevated HbA2 in a Vietnamese Heterozygote

The New -474(C→T) Substitution Discovered in the HBG2 Promoter of a Sardinian δβ-Thalassemia Carrier

(2016) Sandro Trova et al.   ACTA HAEMATOLOGICA

Genotype–phenotype correlation and report of novel mutations in β-globin gene in thalassemia patients

(2015) Rachana Nagar et al.   BLOOD CELLS MOLECULES AND DISEASES

A new unstable variant of the fetal hemoglobinHBG2gene: Hb F-Turritana [Gγ64(E8)Gly→Asp, HBG2:c.194G>A] foundin cisto the Hb F-Sardinia gene [Aγ(E19)Ile→Thr, HBG1:c.227T>C]

(2014) Monica Pirastru et al.   EUROPEAN JOURNAL OF HAEMATOLOGY

Hemoglobin Constant Spring is markedly high in women of an ethnic minority group in Vietnam: A community-based survey and hematologic features

(2013) Van Hoa Nguyen et al.   BLOOD CELLS MOLECULES AND DISEASES

Thalassemia and Hemoglobinopathies in Thua Thien Hue Province, Central Vietnam

(2013) Hoa Van Nguyen et al.   HEMOGLOBIN

Distinctive Mutation Spectrum of theHBBGene in an Urban Eastern Indian Population

(2013) Subhransu Sekhar Sahoo et al.   HEMOGLOBIN

The β-globin promoter −71 C>T mutation is a β+ thalassemic allele

(2011) Shoaib Al Zadjali et al.   EUROPEAN JOURNAL OF HAEMATOLOGY

Large scale screening for haemoglobin disorders in southern Vietnam: implications for avoidance and management

(2010) Sean O’Riordan et al.   BRITISH JOURNAL OF HAEMATOLOGY

Beta-thalassemia

(2010) Antonio Cao et al.   GENETICS IN MEDICINE