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
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.