Associated Papers
Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family.
Seselgyte R et al.
Journal of Dental Research, 2019
Mutation analysis of FOXF2 in patients with disorders of sex development (DSD) in combination with cleft palate.
Jochumsen U et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation, 2008
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