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Background publications
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Gilissen, Arts, Hoischen, Spruijt, Mans, Arts, van Lier, Steehouwer, van Reeuwijk, Kant, Roepman, Knoers, Veltman, Brunner: "Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome." in: American journal of human genetics, Vol. 87, Issue 3, pp. 418-23, 2010 (PubMed).
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