Prenatal screening and diagnosis—An introduction
Prenatal diagnosis using cell-free nucleic acids in maternal body fluids: A decade of progress
Aneuploidy screening in the first trimester
Major fetal structural malformations: The role of new imaging modalities
First trimester ultrasonography in screening and detection of fetal anomalies
The second trimester genetic sonogram
Prenatal diagnosis of structural cardiac defects
From new screens to discovered genes: The successful past and promising present of single gene disorders
Molecular cytogenetic and rapid aneuploidy detection methods in prenatal diagnosis
Ethical considerations of early (first vs. second trimester) risk assessment disclosure for trisomy 21 and patient choice in screening versus diagnostic testing