Jennifer M Broughan, Ben Wreyford, Danielle Martin, Gabriella Melis, Kay Randall, Ewoma Obaro, John Broggio, Nicholas Aldridge, Sylvia Stoianova, Chloe Johnson, Donna Gibbard, Sarah Stevens, Kate M Fleming
PURPOSE: The National Congenital Anomaly and Rare Disease Registration Service (NCARDRS), part of National Disease Registration Service in National Health Service England, quality assures, curates and analyses individual data on the pregnancies, fetuses, babies, children and adults with congenital anomalies and rare diseases across England. The congenital anomaly (CA) register provides a resource for patients and their families, clinicians, researchers and public health professionals in furthering the understanding of CAs...
January 12, 2024: BMJ Open