Pharmacokinetic Evaluation of the Interaction between Hepatitis C Virus Protease Inhibitor Boceprevir and 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Inhibitors Atorvastatin an... by HULSKOTTE, E. G. J, FENG, H.-P, XUAN, F, GUPTA, S, VAN ZUTVEN, M. G. J. A, O'MARA, E, WAGNER, J. A, BUTTERTON, J. R

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A subtype of childhood acute lymphoblastic leukaemia with poor treatment outcome: a genome-wide classification study by Den Boer, Monique L, Dr, van Slegtenhorst, Marjon, PhD, De Menezes, Renée X, PhD, Cheok, Meyling H, PhD, Buijs-Gladdines, Jessica GCAM, BSc, Peters, Susan TCJM, BSc, Van Zutven, Laura JCM, PhD, Beverloo, H Berna, PhD, Van der Spek, Peter J, Prof, Escherich, Gaby, PhD, Horstmann, Martin A, Prof, Janka-Schaub, Gritta E, Prof, Kamps, Willem A, Prof, Evans, William E, Prof, Pieters, Rob, Prof

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Estimates of live birth prevalence of children with Down syndrome in the period 1991–2015 in the Netherlands by Graaf, G., Engelen, J. J. M., Gijsbers, A. C. J., Hochstenbach, R., Hoffer, M. J. V., Kooper, A. J. A., Sikkema‐Raddatz, B., Srebniak, M. I., Kevie‐Kersemaekers, A. M. F., Zutven, L. J. C. M., Voorhoeve, E.

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N-Acetylglutamate Synthase Deficiency Due to a Recurrent Sequence Variant in the N-acetylglutamate Synthase Enhancer Region by Williams, Monique, Burlina, Alberto, Rubert, Laura, Polo, Giulia, Ruijter, George J. G., van den Born, Myrthe, Rüfenacht, Véronique, Haskins, Nantaporn, van Zutven, Laura J. C. M., Tuchman, Mendel, Saris, Jasper J., Häberle, Johannes, Caldovic, Ljubica

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Health Problems in Adults with Prader-Willi Syndrome of Different Genetic Subtypes: Cohort Study, Meta-Analysis and Review of the Literature by Rosenberg, Anna G W, Wellink, Charlotte M, Tellez Garcia, Juan M, Pellikaan, Karlijn, Van Abswoude, Denise H, Davidse, Kirsten, Van Zutven, Laura J C M, Brüggenwirth, Hennie T, Resnick, James L, Van der Lely, Aart J, De Graaff, Laura C G

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The Diagnostic Journey of a Patient with Prader–Willi-Like Syndrome and a Unique Homozygous SNURF-SNRPN Variant; Bio-Molecular Analysis and Review of the Literature by Pellikaan, Karlijn, van Woerden, Geeske M., Kleinendorst, Lotte, Rosenberg, Anna G. W., Horsthemke, Bernhard, Grosser, Christian, van Zutven, Laura J. C. M., van Rossum, Elisabeth F. C., van der Lely, Aart J., Resnick, James L., Brüggenwirth, Hennie T., van Haelst, Mieke M., de Graaff, Laura C. G.

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Identification of NUP98 abnormalities in acute leukemia: JARID1A (12p13) as a new partner gene by van Zutven, Laura J. C. M., Önen, Emine, Velthuizen, Sandra C. J. M., van Drunen, Ellen, von Bergh, Anne R. M., van den Heuvel-Eibrink, Marry M., Veronese, Angelo, Mecucci, Cristina, Negrini, Massimo, de Greef, Georgine E., Beverloo, H. Berna

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Mixoploidy combined with aneuploidy in a 13 year‐old patient with severe multiple congenital abnormalities and intellectual disability by van Zutven, Laura J. C. M., Mancini, Grazia M. S., Bindels‐de Heus, Karen G. C. B., van den Akker, Erica L. T., Hulsman, Lorette O. M., Smit, Marjan, Berna Beverloo, H.

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Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation by HAGENS, Olivier, DUBOS, Aline, VAN BOKHOVEN, Hans, GECZ, Jozef, DOLLFUS, Hélène, ROPERS, Hans-Hilger, SCHWARTZ, Charles E, DE CASSIA STOCCO DOS SANTOS, Rita, KALSCHEUER, Vera, HANAUER, André, ABIDI, Fatima, BARBI, Gotthold, VAN ZUTVEN, Laura, HOELTZENBEIN, Maria, TOMMERUP, Niels, MORAINE, Claude, FRYNS, Jean-Pierre, CHELLY, Jamel

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Estimates of live birth prevalence of children with D own syndrome in the period 1991–2015 in the N etherlands by de Graaf, G., Engelen, J. J. M., Gijsbers, A. C. J., Hochstenbach, R., Hoffer, M. J. V., Kooper, A. J. A., Sikkema‐Raddatz, B., Srebniak, M. I., van der Kevie‐Kersemaekers, A. M. F., van Zutven, L. J. C. M., Voorhoeve, E.

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