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HARVARD Citation
Birgmeier, J. et al. (2018). Biallelic loss‐of‐function WNT5A mutations in an infant with severe and atypical manifestations of Robinow syndrome. American journal of medical genetics. 176 (4), pp. 1030-1036. [Online].
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Birgmeier, J. et al. (2018). Biallelic loss‐of‐function WNT5A mutations in an infant with severe and atypical manifestations of Robinow syndrome. American journal of medical genetics. 176 (4), pp. 1030-1036. [Online].