Published in
Wiley, The American Journal of Medical Genetics - Part A, 9(173), p. 2489-2493, 2017
DOI: 10.1002/ajmg.a.38331
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FOXC1 haploinsufficiency due to 6p25 deletion in a patient with rapidly progressing aortic valve disease
Journal article published in 2017 by
Caroline Ovaert 
,
Tiffany Busa ,
Emilie Faure,
Chantal Missirian,
Nicole Philip,
Florent Paoli,
Mathieu Milh,
Loic Macé,
Stephane Zaffran
,
Tiffany Busa ,
Emilie Faure,
Chantal Missirian,
Nicole Philip,
Florent Paoli,
Mathieu Milh,
Loic Macé,
Stephane Zaffran
This paper is available in a repository.
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