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3. Contributors

5. DNA methylation episignature for Witteveen-Kolk syndrome due to SIN3A haploinsufficiency

11. ClinPhen extracts and prioritizes patient phenotypes directly from medical records to expedite genetic disease diagnosis

13. Raine syndrome: Prenatally identified severe craniofacial phenotype with multisuture synostosis and brain abnormalities associated with variants in FAM20C.

14. Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletions

16. Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletions.

17. List of Contributors

18. Contributors

26. Clinical and molecular characterization of five new individuals with WAC‐related intellectual disability: Evidence of pathogenicity for a novel splicing variant.

27. Leiomyomatosis in an Infant With a SUFUSplice Site Variant: Case Report

30. Transcriptome-wide outlier approach identifies individuals with minor spliceopathies.

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