1. Long‐read genome sequencing resolves a complex 13q structural variant associated with syndromic anophthalmia. Issue 5 (5th February 2022) Authors: Boerkoel, Pierre K.; Dixon, Katherine; Fitzsimons, Carrie; Shen, Yaoqing; Huynh, Stephanie; Schlade‐Bartusiak, Kamilla; Culibrk, Luka; Chan, Simon; Boerkoel, Cornelius F.; Jones, Steven J. M.; Chin, Hui‐Lin Journal: American journal of medical genetics Issue: Volume 188:Issue 5(2022) Page Start: 1589 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗