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Department of Hematogenetics

  1. Screening for β-thalassemia.
  2. Investigating families with various types of thalassemias and hemoglobinopathies.
  3. Molecular characterization of β -thalassemia, α - thalassemia, δ β thalassemia and HPFH.
  4. Prenatal diagnosis for β -thalassemia and other hemoglobinopathies in the first and second trimester of pregnancies.
  5. Diagnosis of red cell enzymopathies in case of hereditary hemolytic anemias. (G6PD, PK, GPI, PFK, PGK).
  6. Investigation in cases of Methoglobinemia (NADH-MR deficiency and Hb abnormalities).
  7. Diagnosis of red cell Membranopathies.