Postnatal
Common genetic disorder carrier status screening for parents
BabyMap - CMA Postnatal
Discover how Chromosomal Microarray (CMA) Postnatal Testing can diagnose genetic disorders in children, helping with developmental delays, intellectual disabilities, and congenital anomalies. Learn more about MapmyGenome's offerings for accurate genetic insights and early intervention.
BabyMap - Newborn screening
NewBorn Screening for IEMs, inherited & rare genetic disorders
FISH - Postnatal
Explore FISH postnatal testing to detect chromosomal abnormalities like trisomies and microdeletions. Discover its clinical utility, when to consider testing, and MapmyGenome’s advanced offerings for rapid, reliable results.
Karyotyping - Postnatal
Postnatal karyotyping helps detect chromosomal abnormalities in individuals with genetic disorders, providing accurate diagnoses and guiding treatment plans. Learn about its clinical utility and when to consider testing.
Whole Exome Sequencing
Discover Whole Exome Sequencing (WES) at MapmyGenome. Our comprehensive genetic test offers detailed insights into ~23,000 protein-coding genes, ideal for diagnosing rare and complex conditions, resolving diagnostic uncertainty, and guiding personalized treatment. Explore our high-precision WES services today.