1. Whole‐exome sequencing revealed a nonsense mutation in STKLD1 causing non‐syndromic pre‐axial polydactyly type A affecting only upper limb. Issue 2 (22nd April 2019) Authors: Umair, Muhammad; Bilal, Muhammad; Ali, Raja H.; Alhaddad, Bader; Ahmad, Farooq; Abdullah, ; Haack, Tobias B.; Alfadhel, Majid; Ansar, Muhammad; Meitinger, Thomas; Ahmad, Wasim Journal: Clinical genetics Issue: Volume 96:Issue 2(2019) Page Start: 134 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗