- Non-invasive prenatal testing (NIPT): Discussing its accuracy, applications, and benefits in screening for common chromosomal abnormalities.
- Diagnostic testing (CVS, amniocentesis): Examining the role of invasive procedures in confirming genetic diagnoses.
- Expanded carrier screening: Highlighting its importance in identifying couples at risk for passing on recessive genetic disorders.
- Fetal exome sequencing: Exploring the use of whole exome sequencing in diagnosing complex fetal anomalies.
- Genetic counseling: Emphasizing its crucial role in helping families understand test results, make informed decisions, and navigate emotional challenges.