Association between phenotype and deletion size in 22q11.2 microdeletion syndrome: systematic review and meta-analysis.
M Fernanda RozasFelipe BenavidesLuis LeónGabriela M RepettoPublished in: Orphanet journal of rare diseases (2019)
The lack of association between deletion size and CHD or PA found in this meta-analysis suggests that deletion size does not explain the incomplete penetrance of these 2 major manifestations, and that the critical region for the development of heart and palatal abnormalities is within LCR A-B, the smallest region of overlap among the three deletion sizes.