Items where authors include "Gilissen, C."

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Souche, E., Beltran, S., Brosens, E. et al. (28 more authors) (2022) Recommendations for whole genome sequencing in diagnostics for rare diseases. European Journal of Human Genetics, 30 (9). pp. 1017-1021. ISSN 1018-4813

Kaplanis, J., Samocha, K.E., Wiel, L. et al. (30 more authors) (2020) Evidence for 28 genetic disorders discovered by combining healthcare and research data. Nature, 586 (7831). pp. 757-762. ISSN 0028-0836

This list was generated on Sat Sep 23 14:52:38 2023 BST.