Genotype-Phenotype Correlation in Patients Suspected of Having Sotos Syndrome von de Boer, Lonneke, Kant, Sarina G., Karperien, Marcel, van Beers, Lotte, Tjon, Jennifer, Vink, Geraldine R., van Tol, Dewy, Dauwerse, Hans, le Cessie, Saskia, Beemer, Frits A., van der Burgt, Ineke, Hamel, Ben C.J., Hennekam, Raoul C., Kuhnle, Ursula, Mathijssen, Inge B., Veenstra-Knol, Hermine E., Schrander Stumpel, Connie T., Breuning, Martijn H., Wit, Jan M.

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Testicular cancer in a patient with Primrose syndrome von Mathijssen, Inge B., van Hasselt-van der Velde, Jos, Hennekam, Raoul C.M.

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Array comparative genomic hybridization analysis of a familial duplication of chromosome 13q: A recognizable syndrome von Mathijssen, Inge B., Hoovers, Jan M.N., Mul, Adri N.P.M., Man, Hai‐Yen, Ket, Jan L., Hennekam, Raoul C.M.

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Iris heterochromia: A variable feature in Verloes-Koulischer-oral-acral syndrome von Mathijssen, Inge B., Fryns, Jean-Pierre, Devriendt, Koen, Sznajer, Yves, Van Eygen, Maurice

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TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromes von Van De Weghe, JC, Giordano, JL, Mathijssen, IB, Mojarrad, M, Lugtenberg, D, Miller, CV, Dempsey, JC, Mohajeri, MSA, van Leeuwen, E, Pajkrt, E, Klaver, CCW, Houlden, H, Eslahi, A, Waters, AM, University of Washington Center for Mendelian Genomics, Bamshad, MJ, Nickerson, DA, Aggarwal, VS, de Vries, BBA, Maroofian, R, Doherty, D

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The Origin of EFNB1 Mutations in Craniofrontonasal Syndrome: Frequent Somatic Mosaicism and Explanation of the Paucity of Carrier Males von Twigg, Stephen R.F., Matsumoto, Kazuya, Kidd, Alexa M.J., Goriely, Anne, Taylor, Indira B., Fisher, Richard B., Hoogeboom, A. Jeannette M., Mathijssen, Irene M.J., Lourenço, M. Teresa, Morton, Jenny E.V., Sweeney, Elizabeth, Wilson, Louise C., Brunner, Han G., Mulliken, John B., Wall, Steven A., Wilkie, Andrew O.M.

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