Pharmacological characterization of a small‐molecule agonist for the chemokine receptor CXCR3 by Scholten, DJ, Canals, M, Wijtmans, M, de Munnik, S, Nguyen, P, Verzijl, D, de Esch, IJP, Vischer, HF, Smit, MJ, Leurs, R

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Specific proteome changes in platelets from individuals with GATA1-, GFI1B-, and RUNX1-linked bleeding disorders by Van Bergen, M.G.J.M., Marneth, A.E., Hoogendijk, A.J., Van Alphen, F.P.J., Van den Akker, E., Laros-Van Gorkom, B.A.P., Hoeks, M., Simons, A., De Munnik, S.A., Janssen, J.J.W.M., Martens, J.H.A., Jansen, J.H., Meijer, A.B., Van der Reijden, B.A.

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An 8.35 Mb overlapping interstitial deletion of 8q24 in two patients with coloboma, congenital heart defect, limb abnormalities, psychomotor retardation and convulsions by Verheij, J.B.G.M, de Munnik, S.A, Dijkhuizen, T, de Leeuw, N, Olde Weghuis, D, van den Hoek, G.J, Rijlaarsdam, R.S, Thomasse, Y.E.M, Dikkers, F.G, Marcelis, C.L.M, van Ravenswaaij-Arts, C.M.A

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Skeletal dysplasia with brachytelephalangy in a patient with a congenital disorder of glycosylation due to ALG6 gene mutations by Drijvers, JM, Lefeber, DJ, De Munnik, SA, Pfundt, R, Van De Leeuw, N, Marcelis, C, Thiel, C, Koerner, C, Wevers, RA, Morava, E

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Toward clinical and molecular understanding of pathogenic variants in the ZBTB18 gene by Schoot, Vyne, Munnik, Sonja, Venselaar, Hanka, Elting, Mariet, Mancini, Grazia M. S., Ravenswaaij‐Arts, Conny M. A., Anderlid, Britt‐Marie, Brunner, Han G., Stevens, Servi J. C.

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Let’s talk about sex: A qualitative study exploring the experiences of HIV nurses when discussing sexual risk behaviours with HIV-positive men who have sex with men by de Munnik, S., den Daas, C., Ammerlaan, H.S.M., Kok, G., Raethke, M.S., Vervoort, S.C.J.M.

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MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype study by Makrythanasis, P, van Bon, BW, Steehouwer, M, Rodríguez-Santiago, B, Simpson, M, Dias, P, Anderlid, BM, Arts, P, Bhat, M, Augello, B, Biamino, E, Bongers, EMHF, del Campo, M, Cordeiro, I, Cueto-González, AM, Cuscó, I, Deshpande, C, Frysira, E, Izatt, L, Flores, R, Galán, E, Gener, B, Gilissen, C, Granneman, SM, Hoyer, J, Yntema, HG, Kets, CM, Koolen, DA, Marcelis, CL, Medeira, A, Micale, L, Mohammed, S, de Munnik, SA, Nordgren, A, Psoni, S, Reardon, W, Revencu, N, Roscioli, T, Ruiterkamp-Versteeg, M, Santos, HG, Schoumans, J, Schuurs-Hoeijmakers, JHM, Silengo, MC, Toledo, L, Vendrell, T, van der Burgt, I, van Lier, B, Zweier, C, Reymond, A, Trembath, RC, Perez-Jurado, L, Dupont, J, de Vries, BBA, Brunner, HG, Veltman, JA, Merla, G, Antonarakis, SE, Hoischen, A

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Health-related quality of life among adult HIV positive patients: assessing comprehensive themes and interrelated associations by den Daas, C., van den Berk, G. E. L., Kleene, M.-J. T., de Munnik, E. S., Lijmer, J. G., Brinkman, K.

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Further delineation of the KBG syndrome caused by ANKRD11 aberrations by Ockeloen, Charlotte W, Willemsen, Marjolein H, de Munnik, Sonja, van Bon, Bregje W M, de Leeuw, Nicole, Verrips, Aad, Kant, Sarina G, Jones, Elizabeth A, Brunner, Han G, van Loon, Rosa L E, Smeets, Eric E J, van Haelst, Mieke M, van Haaften, Gijs, Nordgren, Ann, Malmgren, Helena, Grigelioniene, Giedre, Vermeer, Sascha, Louro, Pedro, Ramos, Lina, Maal, Thomas J J, van Heumen, Celeste C, Yntema, Helger G, Carels, Carine E L, Kleefstra, Tjitske

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Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations by Ockeloen, Charlotte W, Willemsen, Marjolein H, de Munnik, Sonja, van Bon, Bregje W M, de Leeuw, Nicole, Verrips, Aad, Kant, Sarina G, Jones, Elizabeth A, Brunner, Han G, van Loon, Rosa L E, Smeets, Eric E J, van Haelst, Mieke M, van Haaften, Gijs, Nordgren, Ann, Malmgren, Helena, Grigelioniene, Giedre, Vermeer, Sascha, Louro, Pedro, Ramos, Lina, Maal, Thomas J J, van Heumen, Celeste C, Yntema, Helger G, Carels, Carine E L, Kleefstra, Tjitske

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The constitutive activity of the virally encoded chemokine receptor US28 accelerates glioblastoma growth by Heukers, Raimond, Fan, Tian Shu, de Wit, Raymond H., van Senten, Jeffrey R., De Groof, Timo W. M., Bebelman, Maarten P., Lagerweij, Tonny, Vieira, Joao, de Munnik, Sabrina M., Smits-de Vries, Laura, van Offenbeek, Jody, Rahbar, Afsar, van Hoorick, Diane, Söderberg-Naucler, Cecilia, Würdinger, Thomas, Leurs, Rob, Siderius, Marco, Vischer, Henry F., Smit, Martine J.

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Dispersion of the HIV-1 Epidemic in Men Who Have Sex with Men in the Netherlands: A Combined Mathematical Model and Phylogenetic Analysis by Bezemer, Daniela, Cori, Anne, Ratmann, Oliver, van Sighem, Ard, Hermanides, Hillegonda S, Dutilh, Bas E, Gras, Luuk, Rodrigues Faria, Nuno, van den Hengel, Rob, Duits, Ashley J, Reiss, Peter, de Wolf, Frank, Fraser, Christophe

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Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing by Janssen, Anouk E. J., Koeck, Rebekka M., Essers, Rick, Cao, Ping, van Dijk, Wanwisa, Drüsedau, Marion, Meekels, Jeroen, Yaldiz, Burcu, van de Vorst, Maartje, de Koning, Bart, Hellebrekers, Debby M. E. I., Stevens, Servi J. C., Sun, Su Ming, Heijligers, Malou, de Munnik, Sonja A., van Uum, Chris M. J., Achten, Jelle, Hamers, Lars, Naghdi, Marjan, Vissers, Lisenka E. L. M., van Golde, Ron J. T., de Wert, Guido, Dreesen, Jos C. F. M., de Die-Smulders, Christine, Coonen, Edith, Brunner, Han G., van den Wijngaard, Arthur, Paulussen, Aimee D. C., Zamani Esteki, Masoud

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Factors associated with presenting late or with advanced HIV disease in the Netherlands, 1996–2014: results from a national observational cohort by Op de Coul, Eline L M, van Sighem, Ard, Brinkman, Kees, Benthem, Birgit H van, Ende, Marchina E van der, Geerlings, Suzanne, Reiss, Peter

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PS1476 APPLICATION OF WHOLE EXOME SEQUENCING FOR PATIENTS WITH INHERITED PLATELET DISORDERS by Stevens‐Kroef, M., Munnik, S., Heerde, W., Brons, P., Saes, J., Schols, S., Simons, A.

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S847 DISTINCT AND COMMON DEREGULATED PATHWAYS IN RUNX1, GATA1 AND GFI1B ASSOCIATED BLEEDING DISORDERS by Bergen, M., Marneth, A., Alphen, F., Jansen, J., Laros‐van Gorkom, B., Schols, S., Munnik, S., Simons, A., Akker, E., Meijer, A., Reijden, B.

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Management of drug interactions with direct‐acting antivirals in Dutch HIV/hepatitis C virus‐coinfected patients: adequate but not perfect by Rijnders, B, Valk, M, Burger, DM, Meer, J. T. M., Nellen, F. J. B., Pajkrt, D., Goorhuis, A., Hovius, J. W., Eden, J., Back, N. K. T., Berkhout, B., Cornelissen, M. T. E., Wintermans, B., Ziekenhuis, Catharina, Beek, E., Jansz, A. R., Tjhie, J., Brouwer, A. E., Erve, R., Keelan‐Pfaf, S., Buiting, A. G. M., Kinderziekenhuis, Emma, Plas, A., Gorp, E. C. M., Beek, J. E. A., Vriesde, M., Zonneveld, L. M., Berg‐Cameron, H. J., Pas, S. D., Elsenburg, L. J. M., Kwa, I. S., Groeneveld, P. H. P., Berg, J. F., Bliek, G. L., Bor, P. C. J., Bloembergen, P., Boer, M. G. J., Jolink, H., Claas, E. C. J., Hollander, J. G., Kastelijns, M., Smit, J. V., Struik‐Kalkman, D., Tearno, C., Loo, I. H. M., Hartingsveld, A. Y., Mutsaers, J. A. E. M., Veen, S. Q., Slotervaart, MC, Vlasblom, D. J., Smits, P. H. M., Houte, D. P. F., Kampschreur, L. M., Kootstra, G. J., Kortmann, W., Cohen Stuart, J. W. T., Diederen, B. M. W., Renckens, R., Blok, W. L., Brouwer, C. J., Geerders, G. F., Kleene, M. J., Meché, I. B., Spelbrink, M., Crevel, R., Ven, A. J. A. M., Rahamat‐Langendoen, J., Swanink, C. M. A., Lelyveld, S. F. L., Soetekouw, R., Prijt, L. M. M., Swaluw, J., Verhagen, D. W. M., Wijk, M., Bakker, M., Kleinnijenhuis, J., Kloeze, E., Vermont, C. L., Boonstra, A., Leer‐Buter, C. C., Oosterheert, J. J., Agtmael, M. A., Bomers, M., Heitmuller, M., Laan, L. M., Ang, C. W., Houdt, R., Pettersson, A. M., Wolfs, T. F. W., Nauta, N., Bezemer, D. O., Sighem, A. I., Boender, T. S., Zaheri, S., Bakker, Y., Koops, J., Kruijne, E., Munjishvili, L., Ruijs, Y., Rutkens, T.

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Diminished Impact of Ethnicity as a Risk Factor for Chronic Kidney Disease in the Current HIV Treatment Era by Schoffelen, Annelot F., Smit, Colette, van Lelyveld, Steven F. L, Vogt, Liffert, Bauer, Martijn P., Reiss, Peter, Hoepelman, Andy I. M., Barth, Roos E.

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Gender differences in the use of cardiovascular interventions in HIV‐positive persons; the D:A:D Study by El‐Sadr, Wafaa, Pradier, Christian, Bonnet, F, Thulin, E, Necsoi, C, Blance, A, Raben, D, Shortman, N, Pijnappel, FJJ, Berkhout, B, Cornelissen, MTE, De Ruyter Ziekenhuis, A, Stegeman, A, Wegdam, MCA, Vriesde, M, Schippers, EF, Eeden, A, Isala, IS, Groeneveld, PHP, Smit, JV, Niekerk, T, Meerkerk, C, Wildenbeest, GS, Weel, J, Hoeksema, K, Sulman, H, Santegoets, RMWJ, Ven, B, Marcelis, JH, Buiting, AGM, Bierman, WFW, Scholvinck, H, Weerd, DA, Ellerbroek, PM, Arends, JE, Elst‐Laurijssen, DHM, Verduyn‐Lunel, F, Hoekstra, P, Bakker, Y, El Berkaoui, A, Rutkens, T, Gaborieau, V, Wittkop, L, Lawson‐Ayayi, S, Desjardin, S, Faure, I, Ferrand, H, Marie, J, Blaizeau, MJ, Decoin, M, Hoy, J, Lau, H, Neaton, J, Thompson, G, Mushatt, D, Baxter, J, Horban, A, Larsen, JF, Shepherd, L, Gottfredsson, M, Mulcahy, F, Yust, I, Burke, M, Elinav, H, Elbirt, D, Miró, JM, Clotet, B, Tural, C, Gutierrez, M, Mateo, G, Thalme, A, Sluzhynska, M, Ippolito, G, Marchetti, GC, Andreoni, M, Bonora, S, Calza, L, Santoro, MM, Saracino, A, Galli, L, Shanyinde, M, Graziano, S, Giacometti, A, Donati, V, Vichi, F, Viscoli, C, Milini, P, Bonadies, G, Maddaloni, L, Viviani, F, Cua, E, Perbost, I, Pillet, S, Battegay, M, Bernasconi, E, Bucher, Hc, Ciuffi, A, Hirsch, HH, Martinez de Tejada, B, Paioni, P

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Skeletal dysplasia with brachytelephalangy in a patient with a congenital disorder of glycosylation due to ALG6 gene mutations by Drijvers, J M, Lefeber, D J, de Munnik, S A, Pfundt, R, van de Leeuw, N, Marcelis, C, Thiel, C, Koerner, C, Wevers, R A, Morava, E

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