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Update on the genetics of differences of sex development (DSD)
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Blepharophimosis-ptosis-epicanthus inversus syndrome plus: deletion 3q22.3q23 in a patient with characteristic facial features and with genital anomalies, spastic diplegia, and speech delay
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Insights into levator muscle dysfunction in a cohort of patients with molecularly confirmed blepharophimosis-ptosis-epicanthus inversus syndrome using high-resolution imaging, anatomic examination and histopathologic examination
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Blepharophimosis-ptosis-epicanthus inversus syndrome
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FOXL2 copy number changes in the molecular pathogenesis of BPES: unique cohort of 17 deletions
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The transcription factor FOXL2 in ovarian function and dysfunction
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- Journal Article
- A1
- open access
Foxl2 gene and the development of the ovary : a story about goat, mouse, fish and woman