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Dive into the research topics of 'Novel KIAA1033/WASHC4 mutations in three patients with syndromic intellectual disability and a review of the literature'. Together they form a unique fingerprint.- Sort by
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Mirna Assoum, Ange Line Bruel, Melissa L. Crenshaw, Julian Delanne, Ingrid M. Wentzensen, Kirsty McWalter, Karin M. Dent, Antonio Vitobello, Paul Kuentz, Julien Thevenon, Yannis Duffourd, Christel Thauvin-Robinet, Laurence Faivre
Research output: Contribution to journal › Article › peer-review