Associated Papers
Shifting the landscape: Dominant C-terminal rare missense FOXL2 variants in non-syndromic primary ovarian failure etiology.
Jordan P et al.
Clinical Genetics, 2024
Next-generation sequencing of 500 POI patients identified novel responsible monogenic and oligogenic variants.
Luo W et al.
Journal of Ovarian Research, 2023
FOXL2 mutations in Chinese families with Blepharophimosis syndrome (BPES).
Fan JY et al.
Translational Research : the Journal of Laboratory and Clinical Medicine, 2011
FOXL2 mutations in Taiwanese patients with blepharophimosis, ptosis, epicanthus inversus syndrome.
Lin WD et al.
Clinical Chemistry and Laboratory Medicine, 2010
FOXL2 mutations and genomic rearrangements in BPES.
Beysen D et al.
Human Mutation, 2009
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