Associated Papers
Genetic burden in neonatal and pediatric-onset pulmonary hypertension: A single-center retrospective study using exome sequencing in a Chinese population.
Chen C et al.
Pediatrics and Neonatology, 2025
Familial Alveolar Capillary Dysplasia With Misalignment of Pulmonary Veins Caused by Paternal FOXF1 Upstream Enhancer Deletion: A Case Report.
Kawasaki H et al.
American Journal of Medical Genetics. Part A, 2025
Maternal mutations of FOXF1 cause alveolar capillary dysplasia despite not being imprinted.
Alsina Casanova M et al.
Human Mutation, 2017
Variable phenotypic presentation of a novel FOXF1 missense mutation in a single family.
Reiter J et al.
Pediatric Pulmonology, 2016
Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins.
Szafranski P et al.
Human Genetics, 2016
Alveolar capillary dysplasia with misalignment of the pulmonary veins: clinical, histological, and genetic aspects.
Slot E et al.
Pulmonary Circulation, 0
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