1. A novel NEUROG3 mutation in neonatal diabetes associated with a neuro‐intestinal syndrome. Issue 3 (22nd September 2017) Authors: Hancili, Suna; Bonnefond, Amélie; Philippe, Julien; Vaillant, Emmanuel; De Graeve, Franck; Sand, Olivier; Busiah, Kanetee; Robert, Jean‐Jacques; Polak, Michel; Froguel, Philippe; Güven, Ayla; Vaxillaire, Martine Journal: Pediatric diabetes Issue: Volume 19:Issue 3(2018) Page Start: 381 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Bilateral galactocele in a male infant with Down syndrome and congenital hypothyroidism. Issue 5 (18th October 2013) Authors: Güven, Ayla; Hancili, Suna Journal: Pediatrics international Issue: Volume 55:Issue 5(2013) Page Start: e116 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic rickets. (11th May 2017) Authors: Guven, Ayla; Al‐Rijjal, Roua A.; BinEssa, Huda A.; Dogan, Durmuş; Kor, Yılmaz; Zou, Minjing; Kaya, Namik; Alenezi, Anwar F.; Hancili, Suna; Tarım, Ömer; Baitei, Essa Y.; Kattan, Walaa E; Meyer, Brian F.; Shi, Yufei Journal: Clinical endocrinology Issue: Volume 87:Number 1(2017) Page Start: 103 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗