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1. Heterozygous loss-of-function SMC3 variants are associated with variable growth and developmental features

2. The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies

3. Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling

4. Mutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5

5. Heterozygous loss-of-functionSMC3variants are associated with variable and incompletely penetrant growth and developmental features

7. De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation

8. The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies.

10. Noncoding copy-number variations are associated with congenital limb malformation

15. Diagnosis of lethal or prenatal‐onset autosomal recessive disorders by parental exome sequencing

17. Prevalence and architecture of de novo mutations in developmental disorders

21. Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

22. De Novo Heterozygous Mutations in SMC3 Cause a Range of Cornelia de Lange Syndrome-Overlapping Phenotypes

23. Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism

29. Diagnosis of lethal or prenatal‐onset autosomal recessive disorders by parental exome sequencing

30. The prevalence of neurodevelopmental disorders in children prenatally exposed to antiepileptic drugs

32. Meier–Gorlin Syndrome: Growth and Secondary Sexual Development of a Microcephalic Primordial Dwarfism Disorder

35. Nicolaides–Baraitser syndrome: Delineation of the phenotype

38. A molecular and clinical study of Larsen syndrome caused by mutations in FLNB

40. CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

44. Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD

45. The phenotype of Sotos syndrome in adulthood: A review of 44 individuals

46. Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

47. Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

48. Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features

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