Prenatal and Stillbirth Sequencing (H-50977)

The aim of the study is to Identify the genes and disease-causing sequence variants that explain causes of prenatally diagnosed congenital anomalies, stillbirth and early pregnancy loss, with or without prenatally identified congenital anomalies and the impact of these tests on prenatal, delivery and postnatal care, also on various stakeholders and reproductive genetic counseling.