1. A case of G1013R FBN1 mutation: A potential genotype–phenotype correlation in severe Marfan syndrome. Issue 6 (21st March 2020) Authors: Willis, Brooke R.; Lee, Mianne; Rethanavelu, Kavitha; Fung, Jasmine L. F.; Wong, Rosanna M. S.; Hui, Peter; Yeung, Kit S.; Lo, Ivan F. M.; Chung, Brian H. Y. Journal: American journal of medical genetics Issue: Volume 182:Issue 6(2020) Page Start: 1329 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗