Associated Papers
Decreased Level of TMEM100 in Neonates With Lethal Lung Developmental Disorders due to Abnormalities in SHH-FOXF1 and TBX4-FGF10 Signaling Pathways.
Bzdęga K et al.
American Journal of Medical Genetics. Part A, 2025
Genetic features of alveolar capillary dysplasia with misalignment of pulmonary veins in Japanese infants.
Ikeda M et al.
Early Human Development, 2025
Genetic basis for childhood interstitial lung disease among Japanese infants and children.
Hayasaka I et al.
Pediatric Research, 2018
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