Novel<i>FOXF1</i>Mutations in Sporadic and Familial Cases of Alveolar Capillary Dysplasia with Misaligned Pulmonary Veins Imply a Role for its DNA Binding DomainPartha Sen, Iveta Valášková, Katarzyna Kołodziejska et al.|Human Mutation|2013Cited by 129
Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotypePrzemysław Szafrański, Paweł Stankiewicz, Qian Liu et al.|Human Genetics|2019Cited by 32