Associated Papers
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
Evaluation of the Genetic Variation Spectrum Related to Corneal Dystrophy in a Large Cohort.
Li W et al.
Frontiers in Cell and Developmental Biology, 2021
33816482 (PubMed )
Supplement: Data_Sheet_1.XLSX › Supplementary_Data_1
Whole-Exome Sequencing Identifies Damaging de novo Variants in Anencephalic Cases.
Wang L et al.
Frontiers in Neuroscience, 2019
Mutation profiles of congenital cataract genes in 21 northern Chinese families.
Zhang XH et al.
Molecular Vision, 2018
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