1. Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance. Issue 2 (4th January 2019) Authors: Woodward, Karen J.; Stampalia, Julie; Vanyai, Hannah; Rijhumal, Hashika; Potts, Kim; Taylor, Fiona; Peverall, Joanne; Grumball, Tanya; Sivamoorthy, Soruba; Alinejad‐Rokny, Hamid; Wray, John; Whitehouse, Andrew; Nagarajan, Lakshmi; Scurlock, Jacqueline; Afchani, Sabine; Edwards, Matthew; Murch, As... Journal: Molecular genetics & genomic medicine Issue: Volume 7:Issue 2(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗