Cite
HARVARD Citation
Ovaert, C. et al. (2017). FOXC1 haploinsufficiency due to 6p25 deletion in a patient with rapidly progressing aortic valve disease. American journal of medical genetics. 173 (9), pp. 2489-2493. [Online].
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Ovaert, C. et al. (2017). FOXC1 haploinsufficiency due to 6p25 deletion in a patient with rapidly progressing aortic valve disease. American journal of medical genetics. 173 (9), pp. 2489-2493. [Online].