1. ADAMTS10-mediated tissue disruption in Weill–Marchesani syndrome. (27th July 2018) Authors: Mularczyk, Ewa J; Singh, Mukti; Godwin, Alan R F; Galli, Francessco; Humphreys, Neil; Adamson, Antony D; Mironov, Aleksandr; Cain, Stuart A; Sengle, Gerhard; Boot-Handford, Ray P; Cossu, Giulio; Kielty, Cay M; Baldock, Clair Journal: Human molecular genetics Issue: Volume 27:Number 21(2018:Nov. 01) Page Start: 3675 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. ADAMTS10-mediated tissue disruption in Weill–Marchesani syndrome. (27th July 2018) Authors: Mularczyk, Ewa J; Singh, Mukti; Godwin, Alan R F; Galli, Francessco; Humphreys, Neil; Adamson, Antony D; Mironov, Aleksandr; Cain, Stuart A; Sengle, Gerhard; Boot-Handford, Ray P; Cossu, Giulio; Kielty, Cay M; Baldock, Clair Journal: Human molecular genetics Issue: Volume 27:Number 21(2018:Nov. 01) Page Start: 3675 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Leri's pleonosteosis, a congenital rheumatic disease, results from microduplication at 8q22.1 encompassing GDF6 and SDC2 and provides insight into systemic sclerosis pathogenesis. Issue 6 (17th January 2014) Authors: Banka, Siddharth; Cain, Stuart A; Carim, Sabrya; Daly, Sarah B; Urquhart, Jill E; Erdem, Günhan; Harris, Jade; Bottomley, Michelle; Donnai, Dian; Kerr, Bronwyn; Kingston, Helen; Superti-Furga, Andreas; Unger, Sheila; Ennis, Holly; Worthington, Jane; Herrick, Ariane L; Merry, Catherine L R; Yue, W... Journal: Annals of the rheumatic diseases Issue: Volume 74:Issue 6(2015) Page Start: 1249 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗