Severe persistent pulmonary hypertension of the newborn and dysmorphic features in neonate with a deletion involving TWIST1 and PHF14: a case report
Crossref DOI link: https://doi.org/10.1186/s13256-017-1402-4
Published Online: 2017-08-17
Published Print: 2017-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Schinagl, Carina
Melum, Guro Reinholt
Rødningen, Olaug Kristin
Bjørgo, Kathrine
Andresen, Jannicke Hanne