Rapid genetic diagnosis of neonatal persistent pulmonary hypertension with a novel FOXF1 mutation-Reference-Cited by-同舟云学术

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Rapid genetic diagnosis of neonatal persistent pulmonary hypertension with a novel FOXF1 mutation

Published:2023-07 Issue:4 Volume:64 Page:484-486
ISSN:1875-9572
Container-title:Pediatrics & Neonatology
language:en
Short-container-title:Pediatrics & Neonatology

Author:

Wu Jeng-Hung^ORCID,Wang Yu-Jui,Liau Jau-Yu,Lee Ni-Chung^ORCID,Wu En-Ting^ORCID

Funder

Ministry of Science and Technology, Taiwan

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference3 articles.

1. Congenital alveolar capillary dysplasia - an unusual cause of respiratory distress in the newborn;Janney;Am J Clin Pathol,1981

2. Alveolar capillary dysplasia with misalignment of the pulmonary veins: clinical, histological, and genetic aspects;Slot;Pulm Circ,2018

3. Critical trio exome benefits in-time decision-making for pediatric patients with severe illnesses;Wu;Pediatr Crit Care Med,2019

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