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Dive into the research topics of 'Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome'. Together they form a unique fingerprint.- Sort by
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David A. Koolen, Jamie M. Kramer, Kornelia Neveling, Willy M. Nillesen, Heather L. Moore-Barton, Frances V. Elmslie, Annick Toutain, Jeanne Amiel, Valérie Malan, Anne Chun Hui Tsai, Sau Wai Cheung, Christian Gilissen, Eugene T.P. Verwiel, Sarah Martens, Ton Feuth, Ernie M.H.F. Bongers, Petra De Vries, Hans Scheffer, Lisenka E.L.M. Vissers, Arjan P.M. De Brouwer
Research output: Contribution to journal › Article › peer-review