CLINICAL GENETICS

  • Clinical  Diagnosis of Genetic Disorders
  • Pre natal Non-Invasive investigations
  • 3D/4D U/S scan for high risk pregnancies
  • Targeted imaging for fetal anamolies (TIFFA)
  • 2D Echo
  • Pre natal Invasive investigations
  • Amniocentesis
  • Chorionic villus sampling
  • Double marker and triple marker test during pregnancy
  • TORCH Profile
  • Genetic counseling and Risk prediction /Recurrence risk for the below mentioned Genetic disorders
  • Down,s Syndrome
  • Klinefelters syndrome
  • Patau’s  syndrome
  • Wilson’s  Disease
  • PCOD
  • Metabolic Defects
  • Congenital Heart Diseases
  • Repeated Abortions
  • BOH

CYTOGENETICS:

  • Karyotyping with G and C banding techniques
  • FISH  for lymphocyte and amniotic fluid cells
  • Spectral Karyotyping analysis (SKY) for detection of chromosomal abnormalities in cancers.

BIOCHEMISTRY :

  • Screening for Metabolic Disorders
  • Screening for High-risk pregnancies
  • Screening Newborns for Inborn Errors of Metabolism
  • Screening for single gene disorders
  • Wilson’s Diseases,
  • Hemoglobinopathies,
  • Muscular Dystrophies
  • Mucopolysacharidoses
  • Routine Biochemical Investigations
  •  liver and kidney function,
  • Reproductive disorders

MOLECULAR BIOLOGY :

  • Genetic testing for the following disorders
  • Beta Thalassemia
  • Wilson’s Disease
  • Periodic Syndrome
  • Myeloproliferative neoplasm and chemoresponse in Leukemia
  • Recurrent Abortions
  • Swyer Syndrome


ENVIRONMENTAL TOXICOLOGY

  • Comet Assay
  • Micronucleus Assay