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
Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF Pathway.
Karolak JA et al.
American Journal of Human Genetics, 2019
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