Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations
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W. Reardon | H. Brunner | A. Mégarbané | D. Wieczorek | M. Puiu | Marcel Martin | S. Rahmann | B. Albrecht | M. Steehouwer | K. Neveling | B. Callewaert | C. Marcelis | A. Kuechler | H. Lüdecke | U. Hehr | A. Hehr | J. Czeschik | Christopher Teller | R. König | B. Schweiger | H. M. F. Riise Stensland | F. von Deimling | C. Voigt | Marie Falkenberg Smeland