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1. Large-scale evaluation of outcomes following a genetic diagnosis in children with severe developmental disorders

4. List of Contributors

6. POU3F3‐related disorder: Defining the phenotype and expanding the molecular spectrum

7. SOX5: Lamb–Shaffer syndrome—A case series further expanding the phenotypic spectrum

8. Expanding the phenotypic spectrum of Chromosome16p13.11 microduplication: A multicentric analysis of 206 patients

11. De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development

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