Predicting hairline fractures in eggs of mature hens von van Mourik, S, Alders, B P G J, Helderman, F, van de Ven, L J F, Groot Koerkamp, P W G

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De afbouw van psychofarmaca na traumatisch hersenletsel: het belang van een leidraad von Alders, J G, Rijnen, S J M, Bus, B A A

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Priorities and possibilities for Dutch responses to Rio von Alders, J.G.M.

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In-Flight Measurement of Aerodynamic Loads on Captive Stores. Description of the Measurement Equipment and Comparison of Results with Data from Other Sources von Alders, G J

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Small-scale poultry and food security in resource-poor settings: A review von Wong, J.T., de Bruyn, J., Bagnol, B., Grieve, H., Li, M., Pym, R., Alders, R.G.

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Duration of second victim symptoms in the aftermath of a patient safety incident and association with the level of patient harm: a cross-sectional study in the Netherlands von Vanhaecht, Kris, Seys, Deborah, Schouten, Loes, Bruyneel, Luk, Coeckelberghs, Ellen, Panella, Massimiliano, Zeeman, Gerda, A H, Mulders I, E M, Hopstaken L, R, Del Canho, C, Lim, C, Diekerhof, J M, Hoppenbrouwers S, T J M, Doreleijers C, A, Groenhuijzen, L, Den Dijker, J, Simons P, M P, Cornelissen N, J C, Derwig J, J, Wennekes M, Driessche M, Van Den, T H, Lim F, K I, So R, J, Blaauw, I, Ten Brummelhuis, R, Withaar, M-J, Van Schie, M, Alders A, J W, Möllers M, G, Schuurman, S, Maas-Engelen, S M T H, Ten Have, J, Rhodius R, M V, Fakkedij T, D G, Van Hasselt, E M, Roosen A, Kris, Vanhaecht, Deborah, Seys, Loes, Schouten, Luk, Bruyneel, Ellen, Coeckelberghs, Massimiliano, Panella, Gerda, Zeeman G

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Survival, Retention, and Selective Proliferation of Lymphocytes Is Mediated by Gingival Fibroblasts von Moonen, Carolyn G J, Alders, Sven T, Bontkes, Hetty J, Schoenmaker, Ton, Nicu, Elena A, Loos, Bruno G, de Vries, Teun J

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A genome-wide DNA methylation signature for SETD1B-related syndrome von Krzyzewska, I M, Maas, S M, Henneman, P, Lip, K V D, Venema, A, Baranano, K, Chassevent, A, Aref-Eshghi, E, van Essen, A J, Fukuda, T, Ikeda, H, Jacquemont, M, Kim, H-G, Labalme, A, Lewis, S M E, Lesca, G, Madrigal, I, Mahida, S, Matsumoto, N, Rabionet, R, Rajcan-Separovic, E, Qiao, Y, Sadikovic, B, Saitsu, H, Sweetser, D A, Alders, M, Mannens, M M A M

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Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes von Wyrwoll, M J, van Walree, E S, Hamer, G, Rotte, N, Motazacker, M M, Meijers-Heijboer, H, Alders, M, Meißner, A, Kaminsky, E, Wöste, M, Krallmann, C, Kliesch, S, Hunt, T J, Clark, A T, Silber, S, Stallmeyer, B, Friedrich, C, van Pelt, A M M, Mathijssen, I B, Tüttelmann, F

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Do fearful eyes activate empathy-related brain regions in individuals with callous traits? von Han, Thida, Alders, Gésine L., Greening, Steven G., Neufeld, Richard W. J., Mitchell, Derek G. V.

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Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia Syndrome von Oud, Machteld M., Tuijnenburg, Paul, Hempel, Maja, van Vlies, Naomi, Ren, Zemin, Ferdinandusse, Sacha, Jansen, Machiel H., Santer, René, Johannsen, Jessika, Bacchelli, Chiara, Alders, Marielle, Li, Rui, Davies, Rosalind, Dupuis, Lucie, Cale, Catherine M., Wanders, Ronald J.A., Pals, Steven T., Ocaka, Louise, James, Chela, Müller, Ingo, Lehmberg, Kai, Strom, Tim, Engels, Hartmut, Williams, Hywel J., Beales, Phil, Roepman, Ronald, Dias, Patricia, Brunner, Han G., Cobben, Jan-Maarten, Hall, Christine, Hartley, Taila, Le Quesne Stabej, Polona, Mendoza-Londono, Roberto, Davies, E. Graham, de Sousa, Sérgio B., Lessel, Davor, Arts, Heleen H., Kuijpers, Taco W.

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DNA methylation episignature, extension of the clinical features, and comparative epigenomic profiling of Hao-Fountain syndrome caused by variants in USP7 von van der Laan, Liselot, Karimi, Karim, Rooney, Kathleen, Lauffer, Peter, McConkey, Haley, Caro, Pilar, Relator, Raissa, Levy, Michael A., Bhai, Pratibha, Mignot, Cyril, Keren, Boris, Briuglia, Silvana, Sobering, Andrew K., Li, Dong, Vissers, Lisenka E.L.M., Dingemans, Alexander J.M., Valenzuela, Irene, Verberne, Eline A., Misra-Isrie, Mala, Zwijnenburg, Petra J.G., Waisfisz, Quinten, Alders, Mariëlle, Sailer, Sebastian, Schaaf, Christian P., Mannens, Marcel M.A.M., Sadikovic, Bekim, van Haelst, Mieke M., Henneman, Peter

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The MJA–Lancet Countdown on health and climate change: Australian policy inaction threatens lives von Zhang, Ying, Beggs, Paul J, Bambrick, Hilary, Berry, Helen L, Linnenluecke, Martina K, Trueck, Stefan, Alders, Robyn, Bi, Peng, Boylan, Sinead M, Green, Donna, Guo, Yuming, Hanigan, Ivan C, Hanna, Elizabeth G, Malik, Arunima, Morgan, Geoffrey G, Stevenson, Mark, Tong, Shilu, Watts, Nick, Capon, Anthony G

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Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations von Connaughton, Dervla M., Dai, Rufeng, Owen, Danielle J., Marquez, Jonathan, Mann, Nina, Graham-Paquin, Adda L., Nakayama, Makiko, Coyaud, Etienne, Laurent, Estelle M.N., St-Germain, Jonathan R., Blok, Lot Snijders, Vino, Arianna, Klämbt, Verena, Deutsch, Konstantin, Wu, Chen-Han Wilfred, Kolvenbach, Caroline M., Kause, Franziska, Ottlewski, Isabel, Schneider, Ronen, Kitzler, Thomas M., Majmundar, Amar J., Buerger, Florian, Onuchic-Whitford, Ana C., Youying, Mao, Kolb, Amy, Salmanullah, Daanya, Chen, Evan, van der Ven, Amelie T., Rao, Jia, Ityel, Hadas, Seltzsam, Steve, Rieke, Johanna M., Chen, Jing, Vivante, Asaf, Hwang, Daw-Yang, Kohl, Stefan, Dworschak, Gabriel C., Hermle, Tobias, Alders, Mariëlle, Bartolomaeus, Tobias, Bauer, Stuart B., Baum, Michelle A., Brilstra, Eva H., Challman, Thomas D., Zyskind, Jacob, Costin, Carrie E., Dipple, Katrina M., Duijkers, Floor A., Ferguson, Marcia, Fitzpatrick, David R., Fick, Roger, Glass, Ian A., Hulick, Peter J., Kline, Antonie D., Krey, Ilona, Kumar, Selvin, Lu, Weining, Marco, Elysa J., Wentzensen, Ingrid M., Mefford, Heather C., Platzer, Konrad, Povolotskaya, Inna S., Savatt, Juliann M., Shcherbakova, Natalia V., Senguttuvan, Prabha, Squire, Audrey E., Stein, Deborah R., Thiffault, Isabelle, Voinova, Victoria Y., Somers, Michael J.G., Ferguson, Michael A., Traum, Avram Z., Daouk, Ghaleb H., Daga, Ankana, Rodig, Nancy M., Terhal, Paulien A., van Binsbergen, Ellen, Eid, Loai A., Tasic, Velibor, Rasouly, Hila Milo, Lim, Tze Y., Ahram, Dina F., Gharavi, Ali G., Reutter, Heiko M., Rehm, Heidi L., MacArthur, Daniel G., Lek, Monkol, Laricchia, Kristen M., Lifton, Richard P., Xu, Hong, Mane, Shrikant M., Sanna-Cherchi, Simone, Sharrocks, Andrew D., Raught, Brian, Fisher, Simon E., Bouchard, Maxime, Khokha, Mustafa K., Shril, Shirlee, Hildebrandt, Friedhelm

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CREBBP mutations in individuals without Rubinstein-Taybi syndrome phenotype von Menke, Leonie A., van Belzen, Martine J., Alders, Marielle, Cristofoli, Francesca, Ehmke, Nadja, Fergelot, Patricia, Foster, Alison, Gerkes, Erica H., Hoffer, Mariëtte J. V., Horn, Denise, Kant, Sarina G., Lacombe, Didier, Leon, Eyby, Maas, Saskia M., Melis, Daniela, Muto, Valentina, Park, Soo-Mi, Peeters, Hilde, Peters, Dorien J. M., Pfundt, Rolph, van Ravenswaaij-Arts, Conny M. A., Tartaglia, Marco, Hennekam, Raoul C. M.

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Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics von Krzyzewska, I M, Alders, M, Maas, S M, Bliek, J, Venema, A, Henneman, P, Rezwan, F I, Lip, K V D, Mul, A N, Mackay, D J G, Mannens, M M A M

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Participation, agency, and youth voice in establishing school gardens: comparing cases from Kenya and Papua New Guinea von Walker, Graham J., Vos, Amy, Monjero, Kenneth, Sikas-Iha, Trudie, Alders, Robyn G.

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De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders von Jia, Xiangbin, Zhang, Shujie, Tan, Senwei, Du, Bing, He, Mei, Qin, Haisong, Chen, Jia, Duan, Xinyu, Luo, Jingsi, Chen, Fei, Ouyang, Luping, Wang, Jian, Chen, Guodong, Yu, Bin, Zhang, Ge, Zhang, Zimin, Lyu, Yongqing, Huang, Yi, Jiao, Jian, Chen, Jin Yun Helen, Swoboda, Kathryn J, Agolini, Emanuele, Novelli, Antonio, Leoni, Chiara, Zampino, Giuseppe, Cappuccio, Gerarda, Brunetti-Pierri, Nicola, Gerard, Benedicte, Ginglinger, Emmanuelle, Richer, Julie, McMillan, Hugh, White-Brown, Alexandre, Hoekzema, Kendra, Bernier, Raphael A, Kurtz-Nelson, Evangeline C, Earl, Rachel K, Meddens, Claartje, Alders, Marielle, Fuchs, Meredith, Caumes, Roseline, Brunelle, Perrine, Smol, Thomas, Kuehl, Ryan, Day-Salvatore, Debra-Lynn, Monaghan, Kristin G, Morrow, Michelle M, Eichler, Evan E, Hu, Zhengmao, Yuan, Ling, Tan, Jieqiong, Xia, Kun, Shen, Yiping, Guo, Hui

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A Case Series of Familial ARID1B Variants Illustrating Variable Expression and Suggestions to Update the ACMG Criteria von van der Sluijs, Pleuntje J, Alders, Mariëlle, Dingemans, Alexander J M, Parbhoo, Kareesma, van Bon, Bregje W, Dempsey, Jennifer C, Doherty, Dan, den Dunnen, Johan T, Gerkes, Erica H, Milller, Ilana M, Moortgat, Stephanie, Regier, Debra S, Ruivenkamp, Claudia A L, Schmalz, Betsy, Smol, Thomas, Stuurman, Kyra E, Vincent-Delorme, Catherine, de Vries, Bert B A, Sadikovic, Bekim, Hickey, Scott E, Rosenfeld, Jill A, Maystadt, Isabelle, Santen, Gijs W E

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Unilateral condylar hyperplasia in hemifacial hyperplasia, is there genetic proof of overgrowth? von Nolte, J.W., Alders, M., Karssemakers, L.H.E., Becking, A.G., Hennekam, R.C.M.

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