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HARVARD Citation
Ranza, E. et al. (2020). Overlapping phenotypes between SHORT and Noonan syndromes in patients with PTPN11 pathogenic variants. Clinical genetics. 98 (1), pp. 10-18. [Online].
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Ranza, E. et al. (2020). Overlapping phenotypes between SHORT and Noonan syndromes in patients with PTPN11 pathogenic variants. Clinical genetics. 98 (1), pp. 10-18. [Online].