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foxf1 protein, human
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Prenatal Detection of a FOXF1 Deletion in a Fetus with ACDMPV and Hydronephrosis.
Rapid genetic diagnosis of neonatal persistent pulmonary hypertension with a novel FOXF1 mutation.
Descriptive images and features of pulmonary vascular disease in a child with a FOXF1 variant.
Novel FOXF1-Stabilizing Compound TanFe Stimulates Lung Angiogenesis in Alveolar Capillary Dysplasia.
Diagnosis and treatment of a child with alveolar capillary dysplasia with misalignment of pulmonary …
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Epidemiology of Surfactant Protein-B Deficiency
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