Institute has an ongoing program for screening inborn errors of metabolism in mental retardation with special reference to amino acid, carbohydrate and mucopolysaccharide metabolism

Services include

  • Screening for Metabolic disorders.
  • Newborn screening for congenital hypothyrodism and congenital adrenal hyperplasia
  • Double Marker  & Triple marker screening for high risk pregnancies
  • Hormonal Analysis for infertility
  • Screening for Wilson’s Disease
  • Routine Biochemical Investigations

Threoninemia-a new metabolic disorder was identified for the first time in the World.Institute of Genetics was the first to start Radio Immuno Assay (RIA) in AP.More than 15,000 cases of hormonal imbalances were studied.


Name Dr. B. Vijaya LakshmiVijaya Laxmi (1)
Curriculum Vitae View
Qualification M.Sc., Ph.D
Designation Assistant Professor & Incharge
Department Clinical Biochemistry
Area of Research
  • Molecular Studies of Thalassemias, Sickle Cell Anemia and other Hemoglobinopathies
  • Molecular Analysis of  Muscular Dystrophies
  • Micro RNA profiling of NTDs
  • Molecular Cancer Biology
  • Molecular Studies of Wilson Disease
  • Nutrigenomics
E-mail ID
Name Ms. M. ShailajaUpload
Qualification Unavailable
Designation Unavailable
Department Unavailable
Area of Research Unavailable
E-mail ID Unavailable

Current Research Scholars