The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity.
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Francesca Forzano | Hui Zou | Susan Chang | Edward Blair | Hülya Kayserili | Flemming Skovby | Susan M. Chang | Ethylin Wang Jabs | R. Hennekam | E. Jabs | J. Hurst | H. Kayserili | E. Blair | R. Schnur | K. Ozono | L. McDaniel | R. Schultz | F. Skovby | H. Zou | F. Hou | F. Forzano | A. Trainer | Jane A Hurst | K. Inui | Raoul C M Hennekam | Norio Sakai | N. Sakai | Sylvie Manouvrier | M. Gordillo | Koji Inui | Keiichi Ozono | Fajian Hou | Alison H Trainer | Kalle O J Simola | Annick Raas-Rothschild | Miriam Gordillo | Roger A Schultz | Hugo Vega | Ricardo Luque | Seher Basaran | Maria L Giovannucci Uzielli | Rhonda E Schnur | Moritz Meins | Lisa D McDaniel | M. Meins | S. Manouvrier | K. Simola | M. L. Uzielli | H. Vega | A. Raas‐Rothschild | S. Başaran | R. Luque | Hui Zou
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