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Kramers, Cornelis, Janssen, Ben J., Knol, Wilma, Hessel, Marleen H. M., Mulder, Wilhelmina M., Dumont, Glenn, van den Brink, Antoinette Maassen, Tichelaar, Jelle
Veröffentlicht in: Kramers , C , Janssen , B J , Knol , W , Hessel , M H M , Mulder , W M , Dumont , G , van den Brink , A M & Tichelaar , J 2017 , ' A Licence to Prescribe ' , British Journal of Clinical Pharmacology , vol. 83 , no. 8 , pp. 1860-1861 . https://doi.org/10.1111/bcp.13257;
2017
Veröffentlicht in: Kramers , C , Janssen , B J , Knol , W , Hessel , M H M , Mulder , W M , Dumont , G , van den Brink , A M & Tichelaar , J 2017 , ' A Licence to Prescribe ' , British Journal of Clinical Pharmacology , vol. 83 , no. 8 , pp. 1860-1861 . https://doi.org/10.1111/bcp.13257;
2017
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Seco, Celia Zazo, Wesdorp, Mieke, Feenstra, Ilse, Pfundt, Rolph, Hehir-Kwa, Jayne Y., Lelieveld, Stefan H., Castelein, Steven, Gilissen, Christian, de Wijs, Ilse J., Admiraal, Ronald J. C., Pennings, Ronald J. E., Kunst, Henricus P. M., van de Kamp, Jiddeke M., Tamminga, Saskia, Houweling, Arjan C., Plomp, Astrid S., Maas, Saskia M., Gans, Pia A. M. de Koning, Kant, Sarina G., de Geus, Christa M., Frints, Suzanna G. M., Vanhoutte, Els K., van Dooren, Marieke F., van den Boogaard, Marie-Jose H., Scheffer, Hans, Nelen, Marcel, Kremer, Hannie, Hoefsloot, Lies, Schraders, Margit, Yntema, Helger G.
Veröffentlicht in: Seco , C Z , Wesdorp , M , Feenstra , I , Pfundt , R , Hehir-Kwa , J Y , Lelieveld , S H , Castelein , S , Gilissen , C , de Wijs , I J , Admiraal , R J C , Pennings , R J E , Kunst , H P M , van de Kamp , J M , Tamminga , S , Houweling , A C , Plomp , A S , Maas , S M , Gans , P A M D K , Kant , S G , de Geus , C M , Frints , S G M , Vanhoutte , E K , van Dooren , M F , van den Boogaard , M-J H , Scheffer , H , Nelen , M , Kremer , H , Hoefsloot , L , Schraders , M & Yntema , H G 2017 , ' The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands ' , European Journal of Human Genetics , vol. 25 , no. 3 , pp. 308-314 . https://doi.org/10.1038/ejhg.2016.182;
2017
Veröffentlicht in: Seco , C Z , Wesdorp , M , Feenstra , I , Pfundt , R , Hehir-Kwa , J Y , Lelieveld , S H , Castelein , S , Gilissen , C , de Wijs , I J , Admiraal , R J C , Pennings , R J E , Kunst , H P M , van de Kamp , J M , Tamminga , S , Houweling , A C , Plomp , A S , Maas , S M , Gans , P A M D K , Kant , S G , de Geus , C M , Frints , S G M , Vanhoutte , E K , van Dooren , M F , van den Boogaard , M-J H , Scheffer , H , Nelen , M , Kremer , H , Hoefsloot , L , Schraders , M & Yntema , H G 2017 , ' The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands ' , European Journal of Human Genetics , vol. 25 , no. 3 , pp. 308-314 . https://doi.org/10.1038/ejhg.2016.182;
2017
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