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
Identification of a novel mutation in the FGF10 gene in a Chinese family with obvious congenital lacrimal duct dysplasia in lacrimo-auriculo-dento-digital syndrome.
Zhang HY et al.
International Journal of Ophthalmology, 2023
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