BabyMap - Postnatal

Tests to detect chromosomal abnormalities, inherited conditions and rare genetic diseases in the baby

BabyMap - Newborn screening

Babymap is a comprehensive NGS based NewBorn Screening for Inborn errors in metabolism(IEM), inherited conditions and other rare genetic disorders with high focus on critical genes in the Newborns

Karyotyping - Postantal

Karyotyping is a cytogenetic test to detect major chromosomal abnormalities, such as structural & numerical aneuploidies

FISH - Postantal

FISH is a cytogenetic test for common chromosomal abnormalities such as Trisomy 13, Trisomy 18, Trisomy 21.

CMA - Postnatal

Chromosomal microarray (CMA) is a microarray technology that analyzes the entire genome, detecting copy number variants (CNVs) which are commonly associated with various genetic disorders.

Whole Exome Sequencing

Whole Exome Sequencing (WES) is a technique for sequencing the exonic regions on the DNA

Whole Exome Sequencing

Whole Exome Sequencing (WES) is a technique for sequencing the exonic regions on the DNA

We have a lot more to offer apart from these tests. Enquire now!

Postnatal