论文信息 - FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signature - 字舞流文

FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signature

F. Alkuraya | A. Bertoli-Avella | A. A. Tayoun | E. Faqeih | A. El-Hattab | Yoshikazu Johmura | Shruti Sinha | A. Al-Maawali | U. Altunoğlu | F. Alhabshan | Naif A. M. Almontashiri | Malak Alghamdi | N. Ordóñez | J. Basto | N. A. Ali | S. Shenbagam | N. Thalange | Amna Al-Futaisi | Hala Abu Subieh | Navin B. Ramakrishna | Fatma Rabea | R. Jain | M. Nakanishi | Azza Al-Shidhani | Peter Bauer | Suliman Khan | Bruno Reversade | Alawi Alsheikh-Ali | Gehad ElGhazali | Tomohiko Ohta | Majid Alfadhel | Nadia Alhashmi | Umar Bin | Mohamad Sahari | Mariana Ferreira | Mari Mori | Aisha Al Shamsi | Mode Al Ojaimi | Said Ahmed Said Al-Kindi | Abdulaziz Al Saman | Hala Tfayli | Mariam Arabi | Simone Khalifeh | Alan Taylor | Revathy Ramachandran | Anju Jacob | Jay W. Shin | Ikram Chekroun | Mohamed Al Marri | Fahad R. Ali