1. Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita. Issue 1 (20th January 2016) Authors: Ekhilevitch, N.; Kurolap, A.; Oz‐Levi, D.; Mory, A.; Hershkovitz, T.; Ast, G.; Mandel, H.; Baris, H.N. Journal: Clinical genetics Issue: Volume 90:Issue 1(2016) Page Start: 84 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗