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You searched for: Author/Creator Willaert, R.

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1. Association of the missense variant p.Arg203Trp in PACS1 as a cause of intellectual disability and seizures. Issue 2 (23rd January 2017)

2. De novo variants in CDK13 associated with syndromic ID/DD: Molecular and clinical delineation of 15 individuals and a further review. Issue 5 (14th April 2018)

5. Expansion and further delineation of the SETD5 phenotype leading to global developmental delay, variable dysmorphic features, and reduced penetrance. Issue 4 (7th January 2018)