Cite
HARVARD Citation
Brioude, F. et al. (2013). CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome. Journal of medical genetics. 50 (12), pp. 823-830. [Online].
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Brioude, F. et al. (2013). CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome. Journal of medical genetics. 50 (12), pp. 823-830. [Online].