1 articles published in Selcuk Medical Journal with the keyword "deletion": Molecular Characterization of Alpha Thalassemia via Multiplex Ligation Dependent Probe Amplification in Konya, Turkey: A Single Center Study
EMİNE GÖKTAŞ, SÜMEYYE ŞANAL, HÜSEYİN TOKGÖZ, AYŞE GÜL ZAMANİ, MAHMUT SELMAN YILDIRIM
2025, Vol 41, Issue 2, Page 61-65
ABSTRACT Objective: Alpha thalassemia is an autosomal recessive hemoglobinopathy characterized by hypochromic microcytic anemia, exhibiting variable clinical phenotypes. Eighty-five percent of cases arise from deletions in the HBA1 or HBA2 genes. The objective of this study is to present the...
