1. Novel OTOA mutations cause autosomal recessive non‐syndromic hearing impairment in Pakistani families. (23rd November 2012) Authors: Lee, K; Chiu, I; Santos‐Cortez, RLP; Basit, S; Khan, S; Azeem, Z; Andrade, PB; Kim, SS; Ahmad, W; Leal, SM Journal: Clinical genetics Issue: Volume 84:Number 3(2013:Sep.) Page Start: 294 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Impact of maternal risk factors on the structure and function of the heart in newborns. (3rd October 2022) Authors: Noerregaard, M; Voegg, R O B; Raja, A A; Sillesen, A S; Joergensen, F S; Basit, S; Boyd, H; Iversen, K K; Bundgaard, H Journal: European heart journal Issue: Volume 43(2022)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Intramuscular haemangioma of vastus lateralis presenting as stiffness of knee in an adolescent patient. (2014) Authors: Wani, H; Bhat, MS; Basit, S; Khursheed, O; Jan, M; Kawoosa, AA Journal: OA orthopaedics Issue: Volume 2(2014) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗