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HARVARD Citation
Niceta, M. et al. (2018). Biallelic mutations in DYNC2LI1 are a rare cause of Ellis‐van Creveld syndrome. Clinical genetics. 93 (3), pp. 632-639. [Online].
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Niceta, M. et al. (2018). Biallelic mutations in DYNC2LI1 are a rare cause of Ellis‐van Creveld syndrome. Clinical genetics. 93 (3), pp. 632-639. [Online].