Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study by Rauch, Anita, Prof, Wieczorek, Dagmar, MD, Graf, Elisabeth, MSc, Wieland, Thomas, MSc, Endele, Sabine, PhD, Schwarzmayr, Thomas, MSc, Albrecht, Beate, MD, Bartholdi, Deborah, MD, Beygo, Jasmin, MSc, Di Donato, Nataliya, MD, Dufke, Andreas, MD, Cremer, Kirsten, MD, Hempel, Maja, MD, Horn, Denise, MD, Hoyer, Juliane, MD, Joset, Pascal, PhD, Röpke, Albrecht, PhD, Moog, Ute, MD, Riess, Angelika, MD, Thiel, Christian T, MD, Tzschach, Andreas, MD, Wiesener, Antje, MD, Wohlleber, Eva, MD, Zweier, Christiane, MD, Ekici, Arif B, PhD, Zink, Alexander M, MSc, Rump, Andreas, PhD, Meisinger, Christa, MD, Grallert, Harald, PhD, Sticht, Heinrich, PhD, Schenck, Annette, PhD, Engels, Hartmut, PhD, Rappold, Gudrun, Prof, Schröck, Evelin, Prof, Wieacker, Peter, Prof, Riess, Olaf, Prof, Meitinger, Thomas, Prof, Reis, André, Prof, Strom, Tim M, Dr

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Studying the Optimal Intravenous Busulfan Exposure in Pediatric Allogeneic Hematopoietic Cell Transplantation (alloHCT) to Improve Clinical Outcomes: A Multicenter Study by Lalmohamed, Arief, PharmD, PhD, Bartelink, Imke, PharmD, PhD, van Reij, Liesbeth, PharmD, Dvorak, Christopher C., MD, Savic, Rada, PhD, Zwaveling, Juliëtte, PharmD, PhD, Bredius, Robbert, MD, PhD, Egberts, Antoine, PharmD, PhD, Bierings, Marc, MD, PhD, Kletzel, Morris, MD, FAAP, MBA, Shaw, Peter, MD, Nath, Christa, PhD, Hempel, Georg, PhD, Ansari, Marc, MD, Krajinovic, Maja, MD, PhD, Gungor, Tayfun, MD, Wynn, Robert F., MD, Veys, Paul, MD, Cuvelier, Geoff, MD, Chiesa, Robert, MD, PhD, Slatter, Mary, MD, Long-Boyle, Janel, PharmD, PhD, Boelens, Jaap, MD, PhD

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