Associated Papers
Esophageal Atresia, an Anomaly of VACTERL Association or Novel Feature of the FGF10 Gene: A Case Report.
Escalante-Reyes M et al.
Molecular Syndromology, 2025
Variants in FGF10 cause early onset of severe childhood interstitial lung disease: A detailed description of four affected children.
Schütz K et al.
Pediatric Pulmonology, 2023
Phenotypic spectrum of FGF10-related disorders: a systematic review.
Bzdega K et al.
Peerj, 2022
New pathogenic variant in the FGF10 gene in the agenesis of lacrimal and salivary gland syndrome: Ophthalmological and genetic study.
Rodrigo MJ et al.
Ophthalmic Genetics, 0
Select a paper to view details