Cite
HARVARD Citation
Gripp, K. et al. (n.d.). Cardiac anomalies in Axenfeld–Rieger syndrome due to a novel FOXC1 mutation12. American journal of medical genetics. 161 (1), pp. 114-119. [Online].
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Gripp, K. et al. (n.d.). Cardiac anomalies in Axenfeld–Rieger syndrome due to a novel FOXC1 mutation12. American journal of medical genetics. 161 (1), pp. 114-119. [Online].