1. A Novel Loss-of-Sclerostin Function Mutation in a First Egyptian Family with Sclerosteosis. (23rd April 2015) Authors: Fayez, Alaaeldin; Aglan, Mona; Esmaiel, Nora; El Zanaty, Taher; Abdel Kader, Mohamed; El Ruby, Mona Other Names: Zustin Jozef Academic Editor. Journal: BioMed research international Issue: Volume 2015(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Two new patients with focal dermal hypoplasia: A novel PORCN variant and insights on the diagnostic considerations. (3rd January 2022) Authors: Elhossini, Rasha Moheb; Abdel‐Hamid, Mohamed S.; Ashaat, Engy; Otaify, Ghada A.; Dawoud, Heba; Elshimy, Khalid; El Ruby, Mona; Aglan, Mona Journal: Congenital anomalies Issue: Volume 62:Number 2(2022) Page Start: 68 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗