Associated Papers
Novel FOXL2 variants in two Chinese families with blepharophimosis, ptosis, and epicanthus inversus syndrome.
Zhao M et al.
Frontiers in Genetics, 2024
The Genetics and Biology of FOXL2.
Tucker EJ
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation, 2022
FOXL2: at the crossroads of female sex determination and ovarian function.
Benayoun BA et al.
Advances in Experimental Medicine and Biology, 2009
Differential functional effects of novel mutations of the transcription factor FOXL2 in BPES patients.
Nallathambi J et al.
Human Mutation, 2008
Select a paper to view details