Chromosomal abnormalities are major cause of human suffering, which are implicated in mental retardation, congenital malformations, dysmorphic features, primary and secondary amenorrhea, reproductive disorders, infertility neoplastic diseases. Cytogenetic evaluation of patients is helpful in the counseling and management of affected individuals and families. Prenatal diagnosis of chromosomal abnormalities in high-risk pregnancies helps in detecting chromosomally abnormal fetuses. Such couples are counseled regarding continuation of pregnancy.
Our state-of-the-art laboratory offers cytogenetic services in a variety of samples with the application of differential chromosome banding techniques and automated image analysis system for karyotyping and FISH (fluorescence in situ hybridization).

General information and list of tests

Case information sheet

Consent form for molecular diagnosis

Consent form for predictive diagnosis

Form-G for prenatal diagnosis