Associated Papers
Identification of novel FOXP1 variants in four unrelated patients with intellectual disability and speech impairment.
Xiang J et al.
Frontiers in Neurology, 2026
Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders.
Reis LM et al.
Human Molecular Genetics, 2021
34046667 (PubMed )
Supplement: supplemental_files_revised_ddab142.pdf
Genetic landscape of isolated pediatric cataracts: extreme heterogeneity and variable inheritance patterns within genes.
Reis LM et al.
Human Genetics, 2019
Sclerocornea-Microphthalmia-Aphakia Complex: Description of Two Additional Cases Associated With Novel FOXE3 Mutations and Review of the Literature.
Quiroz-Casian N et al.
Cornea, 2018
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