Cite
HARVARD Citation
Torun, D. et al. (2021). Coexistence of severe developmental delay, epilepsy, and hemangioma in Snijders Blok‐Fisher syndrome suggests the presence of a POU3F3‐related SNIBFIS endophenotype: A case report. American journal of medical genetics. 185 (5), pp. 1554-1560. [Online].