Answer:
The correct answer is - a) biochemical separation, identification, and quantification of mixture components.
Step-by-step explanation:
Most hemoglobin disorders can be diagnosed by molecular diagnostic techniques such as protein-based techniques like electrophoresis and chromatography. Protein-based methods can diagnose early thalassemia disorders and hemoglobinopathies but in the case of α-thalassemia may be masked in the presence of β-thalassemia.
Molecular genetic testing plays a very important role in the biochemical separation of molecules or components, identification, and quantification of individuals carrying thalassemia and hemoglobinopathies traits and other hemoglobin disorders.