Associated Papers
Utilization of multiple genetic methods for prenatal diagnosis of rare thalassemia variants.
Jiang F et al.
Frontiers in Genetics, 2023
A Novel -72 (T→A) β-Promoter Mutation Causing Slightly Elevated HbA2 in a Vietnamese Heterozygote.
Pirastru M et al.
Biomed Research International, 2017
Occurrence of the Codon 24 (A > T) Mutation in the Mauritanian Population.
Veten F et al.
Hemoglobin, 2015
Detection of 100% of mutations in 124 individuals using a standard UV/Vis microplate reader: a novel concept for mutation scanning.
Tabone T et al.
Nucleic Acids Research, 2006
Select a paper to view details