Related Articles
α‑thalassemia deletion [‑<sup>SEA</sup> (Southeast Asian)] and a compound heterozygote for the Chinese <sup>G</sup>γ<sup>+</sup>(<sup>A</sup>γδβ)<sup>0</sup>/β<sup>CD17</sup>‑thalassemia mutation: A case report
Impact of genotype on endocrinal complications in β‑thalassemia patients
Novel CC2D2A compound heterozygous mutations cause Joubert syndrome
Bone marrow transplantation in a Hunter patient with P266H mutation.
Novel compound heterozygous mutations in the SPTA1 gene, causing hereditary spherocytosis in a neonate with Coombs‑negative hemolytic jaundice