1. Novel homozygous SLC29A3 mutations among two unrelated Egyptian families with spectral features of H‐syndrome. Issue 4 (4th June 2014) Authors: Al‐Haggar, Mohammad; Salem, Nanees; Wahba, Yahya; Ahmad, Nermin; Jonard, Laurence; Abdel‐Hady, Dina; El‐Hawary, Amany; El‐Sharkawy, Ashraf; Eid, Abdel‐Rhman; El‐Hawary, Amira Journal: Pediatric diabetes Issue: Volume 16:Issue 4(2015:Jul.) Page Start: 305 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Partial expression of ornithine transcarbamylase deficiency in an Egyptian female carrier. Issue 2 (31st October 2013) Authors: Al‐Haggar, Mohammad; Largiadèr, Carlo R.; Abdel‐Hady, Dina; Barakat, Tarik; Nuoffer, Jean‐Marc; Al‐Refaei, Abdel‐Aziz Journal: International journal of gynaecology and obstetrics Issue: Volume 124:Issue 2(2014) Page Start: 174 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗