PMC · DOI:10.3389/fgene.2024.1414939·April 29, 2024
Corrigendum: Novel FOXL2 variants in two Chinese families with blepharophimosis, ptosis, and epicanthus inversus syndrome
Mingyu Zhao, Xiaolu Meng, Jiaqi Wang, Tailing Wang
Abstract
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Taxonomy
TopicsGenetics and Neurodevelopmental Disorders · Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities · Sexual Differentiation and Disorders