Entries of von Deimling, Florian on the publication server
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Number of items: 1.
2013
Voigt, Claudia, Mégarbané, André, Neveling, Kornelia, Czeschik, Johanna Christina 
, Albrecht, Beate, Callewaert, Bert , von Deimling, Florian, Hehr, Andreas, Falkenberg Smeland, Marie, König, Rainer, Kuechler, Alma, Marcelis, Carlo, Puiu, Maria, Reardon, Willie, Riise Stensland, Hilde Monica Frostad, Schweiger, Bernd , Steehouwer, Marloes, Teller, Christopher, Martin, Marcel , Rahmann, Sven, Hehr, Ute, Brunner, Han G, Lüdecke, Hermann-Josef and Wieczorek, Dagmar
(2013)
Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations.
Orphanet Journal of Rare Diseases 8 (1).
Fulltext not available.
, Albrecht, Beate, Callewaert, Bert , von Deimling, Florian, Hehr, Andreas, Falkenberg Smeland, Marie, König, Rainer, Kuechler, Alma, Marcelis, Carlo, Puiu, Maria, Reardon, Willie, Riise Stensland, Hilde Monica Frostad, Schweiger, Bernd , Steehouwer, Marloes, Teller, Christopher, Martin, Marcel , Rahmann, Sven, Hehr, Ute, Brunner, Han G, Lüdecke, Hermann-Josef and Wieczorek, Dagmar
(2013)
Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations.
Orphanet Journal of Rare Diseases 8 (1).
Fulltext not available.