development of solid spectral filters for the regulation of plant growth by Van Haeringen, C.J, Davis, F.J, West, J.S, Gilbert, A, Hadley, P, Pearson, S, Wheldon, A.E, Henbest, R.G.C

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Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome by Celli, Jacopo, Duijf, Pascal, Hamel, Ben C.J, Bamshad, Michael, Kramer, Bridget, Smits, Arie P.T, Newbury-Ecob, Ruth, Hennekam, Raoul C.M, Van Buggenhout, Griet, van Haeringen, Arie, Woods, C.Geoffrey, van Essen, Anthonie J, de Waal, Rob, Vriend, Gert, Haber, Daniel A, Yang, Annie, McKeon, Frank, Brunner, Han G, van Bokhoven, Hans

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Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals by Bijlsma, E.K, Gijsbers, A.C.J, Schuurs-Hoeijmakers, J.H.M, van Haeringen, A, Fransen van de Putte, D.E, Anderlid, B.-M, Lundin, J, Lapunzina, P, Pérez Jurado, L.A, Delle Chiaie, B, Loeys, B, Menten, B, Oostra, A, Verhelst, H, Amor, D.J, Bruno, D.L, van Essen, A.J, Hordijk, R, Sikkema-Raddatz, B, Verbruggen, K.T, Jongmans, M.C.J, Pfundt, R, Reeser, H.M, Breuning, M.H, Ruivenkamp, C.A.L

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Dual origins of dairy cattle farming--evidence from a comprehensive survey of European Y-chromosomal variation by Edwards, Ceiridwen J, Ginja, Catarina, Kantanen, Juha, Pérez-Pardal, Lucía, Tresset, Anne, Stock, Frauke, Gama, Luis T, Penedo, M Cecilia T, Bradley, Daniel G, Lenstra, Johannes A, Nijman, Isaäc J

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A terminal 3p26.3 deletion is not associated with dysmorphic features and intellectual disability in a four-generation family by Moghadasi, Setareh, van Haeringen, Arie, Langendonck, Lieke, Gijsbers, Antoinet C. J., Ruivenkamp, Claudia A. L.

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A new diagnostic workflow for patients with mental retardation and or multiple congenital abnormalities: test arrays first by Gijsbers, Antoinet CJ, Lew, Janet YK, Bosch, Cathy AJ, Schuurs-Hoeijmakers, Janneke HM, van Haeringen, Arie, den Hollander, Nicolette S, Kant, Sarina G, Bijlsma, Emilia K, Breuning, Martijn H, Bakker, Egbert, Ruivenkamp, Claudia AL

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X-chromosome duplications in males with mental retardation: pathogenic or benign variants? by Gijsbers, ACJ, Den Hollander, NS, Helderman-van de Enden, ATJM, Schuurs-Hoeijmakers, JHM, Vijfhuizen, L, Bijlsma, EK, Van Haeringen, A, Hansson, KBM, Bakker, E, Breuning, MH, Ruivenkamp, CAL

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Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63 by MCGRATH, John A, DUIJF, Pascal H. G, ORLOW, Seth J, VAN HAERINGEN, Arie, AUSEMS, Margreet G. E. M, YANG, Annle, MCKEON, Frank, BAMSHAD, Michael A, BRUNNER, Han G, HAMEL, Ben C. J, VAN BOKHOVEN, Hans, DOETSCH, Volker, IRVINE, Alan D, DE WAAL, Rob, VANMOLKOT, Kaate R. J, WESSAGOWIT, Vesarat, KELLY, Alexander, ATHERTON, David J, GRIFFITHS, W. Andrew D

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Additional cryptic CNVs in mentally retarded patients with apparently balanced karyotypes by Gijsbers, Antoinet C.J, Bosch, Cathy A.J, Dauwerse, Johannes G, Giromus, Osdilly, Hansson, Kerstin, Hilhorst-Hofstee, Yvonne, Kriek, Marjolein, van Haeringen, Arie, Bijlsma, Emilia K, Bakker, Egbert, Breuning, Martijn H, Ruivenkamp, Claudia A.L

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