A population study of chromosome 22q11 deletions in infancy

1998250 citationsJournal Articlebronze Open Access

Authors

Judith Goodship · Freeman Hospital

I Cross · Freeman Hospital

Jesse Li‐Ling · Freeman Hospital

Christopher Wren · Freeman Hospital

Abstract

The most common chromosomal cause of significant congenital heart disease remains trisomy 21, while the second most common chromosomal cause is deletion in chromosome band 22q11.

Topics & Keywords

Congenital heart defects research Congenital Heart Disease Studies Genomic variations and chromosomal abnormalities

UN Sustainable Development Goals

Good health and well-being

Publication Details

Published in: Archives of Disease in Childhood

Volume 79, Issue 4, pp. 348-351

DOI: 10.1136/adc.79.4.348

Field-Weighted Citation Impact: 1.32