Development and progress of the National Congenital Anomaly and Rare Disease Registration Service

Sarah Stevens*, Nicola Miller, Jeremy Rashbass

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)
Original languageEnglish
Pages (from-to)215-218
Number of pages4
JournalArchives of Disease in Childhood
Issue number3
Publication statusPublished - Mar 2018


  • congenital abnorm
  • data collection
  • disease registration
  • public health
  • rare disease

Cite this