{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T14:59:55Z","timestamp":1761749995070,"version":"build-2065373602"},"reference-count":3,"publisher":"Elsevier BV","issue":"4","license":[{"start":{"date-parts":[[2023,7,1]],"date-time":"2023-07-01T00:00:00Z","timestamp":1688169600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2023,7,1]],"date-time":"2023-07-01T00:00:00Z","timestamp":1688169600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2023,1,21]],"date-time":"2023-01-21T00:00:00Z","timestamp":1674259200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100004663","name":"Ministry of Science and Technology, Taiwan","doi-asserted-by":"publisher","award":["108-2321-B-002-050-"],"award-info":[{"award-number":["108-2321-B-002-050-"]}],"id":[{"id":"10.13039\/501100004663","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","pediatr-neonatol.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Pediatrics & Neonatology"],"published-print":{"date-parts":[[2023,7]]},"DOI":"10.1016\/j.pedneo.2022.12.010","type":"journal-article","created":{"date-parts":[[2023,1,25]],"date-time":"2023-01-25T07:57:43Z","timestamp":1674633463000},"page":"484-486","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":4,"title":["Rapid genetic diagnosis of neonatal persistent pulmonary hypertension with a novel FOXF1 mutation"],"prefix":"10.1016","volume":"64","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-7505-3516","authenticated-orcid":false,"given":"Jeng-Hung","family":"Wu","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yu-Jui","family":"Wang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jau-Yu","family":"Liau","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5011-7499","authenticated-orcid":false,"given":"Ni-Chung","family":"Lee","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1463-8721","authenticated-orcid":false,"given":"En-Ting","family":"Wu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.pedneo.2022.12.010_bib1","doi-asserted-by":"crossref","first-page":"722","DOI":"10.1093\/ajcp\/76.5.722","article-title":"Congenital alveolar capillary dysplasia - an unusual cause of respiratory distress in the newborn","volume":"76","author":"Janney","year":"1981","journal-title":"Am J Clin Pathol"},{"key":"10.1016\/j.pedneo.2022.12.010_bib2","doi-asserted-by":"crossref","DOI":"10.1177\/2045894018795143","article-title":"Alveolar capillary dysplasia with misalignment of the pulmonary veins: clinical, histological, and genetic aspects","volume":"8","author":"Slot","year":"2018","journal-title":"Pulm Circ"},{"key":"10.1016\/j.pedneo.2022.12.010_bib3","doi-asserted-by":"crossref","first-page":"1021","DOI":"10.1097\/PCC.0000000000002068","article-title":"Critical trio exome benefits in-time decision-making for pediatric patients with severe illnesses","volume":"20","author":"Wu","year":"2019","journal-title":"Pediatr Crit Care Med"}],"container-title":["Pediatrics & Neonatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1875957223000189?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1875957223000189?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T14:57:11Z","timestamp":1761749831000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1875957223000189"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,7]]},"references-count":3,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2023,7]]}},"alternative-id":["S1875957223000189"],"URL":"https:\/\/doi.org\/10.1016\/j.pedneo.2022.12.010","relation":{},"ISSN":["1875-9572"],"issn-type":[{"type":"print","value":"1875-9572"}],"subject":[],"published":{"date-parts":[[2023,7]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Rapid genetic diagnosis of neonatal persistent pulmonary hypertension with a novel FOXF1 mutation","name":"articletitle","label":"Article Title"},{"value":"Pediatrics & Neonatology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.pedneo.2022.12.010","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"simple-article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2023 Taiwan Pediatric Association. Published by Elsevier Taiwan LLC.","name":"copyright","label":"Copyright"}]}}