{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,8,28]],"date-time":"2025-08-28T12:05:34Z","timestamp":1756382734393},"reference-count":14,"publisher":"Springer Science and Business Media LLC","issue":"4","license":[{"start":{"date-parts":[[2014,3,28]],"date-time":"2014-03-28T00:00:00Z","timestamp":1395964800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.springer.com\/tdm"},{"start":{"date-parts":[[2014,3,28]],"date-time":"2014-03-28T00:00:00Z","timestamp":1395964800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["J Perinatol"],"published-print":{"date-parts":[[2014,4]]},"DOI":"10.1038\/jp.2013.175","type":"journal-article","created":{"date-parts":[[2014,3,28]],"date-time":"2014-03-28T07:21:34Z","timestamp":1395991294000},"page":"326-328","update-policy":"http:\/\/dx.doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":4,"title":["Alveolar capillary dysplasia with multiple congenital anomalies and bronchoscopic airway abnormalities"],"prefix":"10.1038","volume":"34","author":[{"given":"V","family":"Bellamkonda-Athmaram","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C G","family":"Sulman","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D G","family":"Basel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J","family":"Southern","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G G","family":"Konduri","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M A","family":"Basir","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2014,3,28]]},"reference":[{"issue":"2","key":"BFjp2013175_CR1","doi-asserted-by":"publisher","first-page":"172","DOI":"10.1164\/rccm.201010-1697CI","volume":"184","author":"NB Bishop","year":"2011","unstructured":"Bishop NB, Stankiewicz P, Steinhorn RH . Alveolar capillary dysplasia. Am J Respir Crit Care Med 2011; 184 (2): 172\u2013179.","journal-title":"Am J Respir Crit Care Med"},{"issue":"6","key":"BFjp2013175_CR2","doi-asserted-by":"publisher","first-page":"43","DOI":"10.1097\/PCC.0b013e31818e383e","volume":"9","author":"S Ahmed","year":"2008","unstructured":"Ahmed S, Ackerman V, Faught P, Langston C . Profound hypoxemia and pulmonary hypertension in a 7-month-old infant: late presentation of alveolar capillary dysplasia. Pediatr Crit Care Med 2008; 9 (6): 43\u201346.","journal-title":"Pediatr Crit Care Med"},{"issue":"2","key":"BFjp2013175_CR3","doi-asserted-by":"publisher","first-page":"177","DOI":"10.1097\/01.PCC.0000202570.58016.67","volume":"7","author":"V Shankar","year":"2006","unstructured":"Shankar V, Haque A, Johnson J, Pietsch J . Late presentation of alveolar capillary dysplasia in an infant. Pediatr Crit Care Med 2006; 7 (2): 177\u2013179.","journal-title":"Pediatr Crit Care Med"},{"issue":"2","key":"BFjp2013175_CR4","doi-asserted-by":"publisher","first-page":"298","DOI":"10.1007\/s00540-010-1080-5","volume":"25","author":"T Shimizu","year":"2011","unstructured":"Shimizu T, Fukuda T, Inomata S, Satsumae T, Tanaka M . A novel association of alveolar capillary dysplasia, atypical duodenal atresia, and subglottic stenosis. J Anesth 2011; 25 (2): 298\u2013300.","journal-title":"J Anesth"},{"issue":"5","key":"BFjp2013175_CR5","doi-asserted-by":"publisher","first-page":"618","DOI":"10.1016\/S0002-9149(99)00395-1","volume":"84","author":"JR Lane","year":"1999","unstructured":"Lane JR, Siwik E, Preminger T, Stork E, Spector M . Prospective diagnosis of alveolar capillary dysplasia in infants with congenital heart disease. Am J Cardiol 1999; 84 (5): 618\u2013620.","journal-title":"Am J Cardiol"},{"issue":"5","key":"BFjp2013175_CR6","doi-asserted-by":"publisher","first-page":"646","DOI":"10.1016\/j.jpeds.2004.06.081","volume":"145","author":"P Sen","year":"2004","unstructured":"Sen P, Thakur N, Stockton DW, Langston C, Bejjani BA . Expanding the phenotype of alveolar capillary dysplasia. J Pediatr 2004; 145 (5): 646\u2013651.","journal-title":"J Pediatr"},{"issue":"6","key":"BFjp2013175_CR7","doi-asserted-by":"publisher","first-page":"780","DOI":"10.1016\/j.ajhg.2009.05.005","volume":"84","author":"P Stankiewicz","year":"2009","unstructured":"Stankiewicz P, Sen P, Bhatt SS, Storer M, Xia Z, Bejjani BA et al. Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations. Am J Hum Genet 2009; 84 (6): 780\u2013791.","journal-title":"Am J Hum Genet"},{"issue":"1","key":"BFjp2013175_CR8","doi-asserted-by":"publisher","first-page":"6","DOI":"10.1016\/j.ejmg.2009.10.001","volume":"53","author":"C Shaw-Smith","year":"2010","unstructured":"Shaw-Smith C . Genetic factors in esophageal atresia, tracheo-esophageal fistula and the VACTERL association: roles for FOXF1 and the 16q24.1 FOX transcription factor gene cluster, and review of the literature. Eur J Med Genet 2010; 53 (1): 6\u201313.","journal-title":"Eur J Med Genet"},{"issue":"9","key":"BFjp2013175_CR9","doi-asserted-by":"publisher","first-page":"5936","DOI":"10.1074\/jbc.M808103200","volume":"284","author":"BB Madison","year":"2009","unstructured":"Madison BB, McKenna LB, Dolson D, Epstein DJ, Kaestner KH . FoxF1 and FoxL1 link hedgehog signaling and the control of epithelial proliferation in the developing stomach and intestine. J Biol Chem 2009; 284 (9): 5936\u20135944.","journal-title":"J Biol Chem"},{"issue":"3","key":"BFjp2013175_CR10","doi-asserted-by":"publisher","first-page":"L521","DOI":"10.1152\/ajplung.00212.2003","volume":"286","author":"VV Kalinichenko","year":"2004","unstructured":"Kalinichenko VV, Gusarova GA, Kim IM, Shin B, Yoder HM, Clark J et al. Foxf1 haploinsufficiency reduces Notch-2 signaling during mouse lung development. Am J Physiol Lung Cell Mol Physiol 2004; 286 (3): L521\u2013L530.","journal-title":"Am J Physiol Lung Cell Mol Physiol"},{"issue":"18","key":"BFjp2013175_CR11","doi-asserted-by":"publisher","first-page":"297","DOI":"10.1242\/dev.010140","volume":"134","author":"J Beh","year":"2007","unstructured":"Beh J, Shi W, Levine M, Davidson B, Christiaen L . FoxF is essential for FGF-induced migration of heart progenitor cells in the ascidian Ciona intestinalis. Development 2007; 134 (18): 297\u2013305.","journal-title":"Development"},{"issue":"3","key":"BFjp2013175_CR12","doi-asserted-by":"publisher","first-page":"163","DOI":"10.1136\/jmedgenet-2012-101288","volume":"50","author":"GR Handrigan","year":"2013","unstructured":"Handrigan GR, Chitayat D, Lionel AC, Pinsk M, Vaags AK, Marshall CR et al. Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation. J Med Genet 2013; 50 (3): 163\u2013173.","journal-title":"J Med Genet"},{"issue":"5","key":"BFjp2013175_CR13","doi-asserted-by":"publisher","first-page":"1257","DOI":"10.1002\/ajmg.a.33378","volume":"152","author":"S Yu","year":"2010","unstructured":"Yu S, Shao L, Kilbride H, Zwick DL . Haploinsufficiencies of FOXF1 and FOXC2 genes associated with lethal alveolar capillary dysplasia and congenital heart disease. Am J Med Genet A 2010; 152 (5): 1257\u20131262.","journal-title":"Am J Med Genet A"},{"issue":"6","key":"BFjp2013175_CR14","doi-asserted-by":"publisher","first-page":"427","DOI":"10.1097\/PCC.0b013e3182192c96","volume":"12","author":"F Zufferey","year":"2011","unstructured":"Zufferey F, Martinet D, Osterheld MC, Niel-B\u00fctschi F, Giannoni E, Besuchet SN et al. 16q24.1 microdeletion in a premature newborn: usefulness of array-based comparative genomic hybridization in persistent pulmonary hypertension of the newborn. Pediatr Crit Care Med 2011; 12 (6): 427\u2013432.","journal-title":"Pediatr Crit Care Med"}],"container-title":["Journal of Perinatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.nature.com\/articles\/jp2013175.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/www.nature.com\/articles\/jp2013175","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/www.nature.com\/articles\/jp2013175.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,3,18]],"date-time":"2022-03-18T13:44:32Z","timestamp":1647611072000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.nature.com\/articles\/jp2013175"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,3,28]]},"references-count":14,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2014,4]]}},"alternative-id":["BFjp2013175"],"URL":"https:\/\/doi.org\/10.1038\/jp.2013.175","relation":{},"ISSN":["0743-8346","1476-5543"],"issn-type":[{"value":"0743-8346","type":"print"},{"value":"1476-5543","type":"electronic"}],"subject":[],"published":{"date-parts":[[2014,3,28]]},"assertion":[{"value":"15 September 2013","order":1,"name":"received","label":"Received","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"29 November 2013","order":2,"name":"revised","label":"Revised","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"3 December 2013","order":3,"name":"accepted","label":"Accepted","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"28 March 2014","order":4,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"The authors declare no conflict of interest.","order":1,"name":"Ethics","group":{"name":"EthicsHeading","label":"Competing interests"}}]}}