The need to perform α-thalassemia genetic testing in Italian patients with β-thalassemia trait: A case report. [PDF]
Santoro G +5 more
europepmc +1 more source
Prevalence of α-thalassemia 3.7 kb deletion in the adult population of Rio Grande do Norte, Brazil
α-Thalassemia, arising from a defect in a-globin chain synthesis, is often caused by deletions involving one or both of the a-genes on the same allele. With the aim of investigating the prevalence of α-thalassemia 3.7 kb deletion in the adult population ...
Gustavo Henrique de Medeiros Alcoforado +7 more
doaj
Detection of maternal carriers of common α-thalassemia deletions from cell-free DNA. [PDF]
Doan PL +36 more
europepmc +1 more source
Analysis of clinical parameters of different types of α-thalassemia children in Hainan region, China. [PDF]
Gao G +10 more
europepmc +1 more source
Advances in the management of α-thalassemia major: reasons to be optimistic. [PDF]
Horvei P, MacKenzie T, Kharbanda S.
europepmc +1 more source
Importance of the 3'UTR region in globin synthesis: identification of two novel HBA1 mutations causing α-Thalassemia. [PDF]
Benito SF +8 more
europepmc +1 more source
Discordantly high glycated hemoglobin might assist in diagnosing α-thalassemia, but not diabetes: A case report. [PDF]
Gao W, Jin Y, Huang Y, Tang H.
europepmc +1 more source
Innovative Rapid Detection System for Nondeletion-Type α‑Thalassemia via Whole-Blood Amplification and Microfluidic Technology. [PDF]
Wei Y +9 more
europepmc +1 more source
Consensus statement for the perinatal management of patients with α thalassemia major. [PDF]
MacKenzie TC +20 more
europepmc +1 more source
Diagnostic Utility of a Multiplex PCR Assay in Detecting Common Mutations of the α-Globin Gene in α-Thalassemia. [PDF]
Park SN, Roh J, Kim JT, Song MJ.
europepmc +1 more source

