FOXL2mutations and genomic rearrangements in BPES
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
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1. CRISPR targeting of FOXL2 c.402C>G mutation reduces malignant phenotype in granulosa tumor cells and identifies anti-tumoral compounds;2024-07-03
2. Novel FOXL2 variants in two Chinese families with blepharophimosis, ptosis, and epicanthus inversus syndrome;Frontiers in Genetics;2024-02-12
3. Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES): Brief review of genetics, clinical presentation, and management;Tropical Ophthalmology;2024-01
4. Expanded phenotypic spectrum of FOXL2 Variant c.672_701dup revealed by whole-exome sequencing in a rare blepharophimosis, ptosis, and epicanthus inversus syndrome family;BMC Ophthalmology;2023-11-07
5. Ovarian Reserve and ART Outcomes in Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Patients With FOXL2 Mutations;Frontiers in Endocrinology;2022-04-28
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