{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,16]],"date-time":"2025-12-16T12:30:19Z","timestamp":1765888219772,"version":"build-2065373602"},"reference-count":37,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2020,2,1]],"date-time":"2020-02-01T00:00:00Z","timestamp":1580515200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2020,2,1]],"date-time":"2020-02-01T00:00:00Z","timestamp":1580515200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Paediatric Respiratory Reviews"],"published-print":{"date-parts":[[2020,2]]},"DOI":"10.1016\/j.prrv.2019.09.004","type":"journal-article","created":{"date-parts":[[2019,10,8]],"date-time":"2019-10-08T18:26:51Z","timestamp":1570559211000},"page":"24-27","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":5,"special_numbering":"C","title":["Genetic factors in isolated and syndromic laryngeal cleft"],"prefix":"10.1016","volume":"33","author":[{"given":"Youjin","family":"Li","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xiaoqing","family":"Rui","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Niu","family":"Li","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.prrv.2019.09.004_b0005","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1186\/1750-1172-6-81","article-title":"Laryngo-tracheo-oesophageal clefts","volume":"6","author":"Leboulanger","year":"2011","journal-title":"Orphanet J Rare Dis"},{"key":"10.1016\/j.prrv.2019.09.004_b0010","doi-asserted-by":"crossref","first-page":"1002","DOI":"10.1177\/000348949710601203","article-title":"Laryngotracheoesophageal clefts","volume":"106","author":"Moungthong","year":"1997","journal-title":"Ann Otol Rhinol Laryngol"},{"key":"10.1016\/j.prrv.2019.09.004_b0015","doi-asserted-by":"crossref","first-page":"2073","DOI":"10.1016\/j.ijporl.2006.07.021","article-title":"Type 1 laryngeal cleft: establishing a functional diagnostic and management algorithm","volume":"70","author":"Chien","year":"2006","journal-title":"Int J Pediatr Otorhinolaryngol"},{"key":"10.1016\/j.prrv.2019.09.004_b0020","doi-asserted-by":"crossref","first-page":"1525","DOI":"10.1016\/j.ijporl.2011.08.020","article-title":"The management of laryngeal clefts","volume":"75","author":"Thiel","year":"2011","journal-title":"Int J Pediatr Otorhinolaryngol"},{"issue":"913\u2013933","key":"10.1016\/j.prrv.2019.09.004_b0025","first-page":"ix","article-title":"Laryngeal cleft","volume":"41","author":"Pezzettigotta","year":"2008","journal-title":"Otolaryngol Clin North Am"},{"key":"10.1016\/j.prrv.2019.09.004_b0030","doi-asserted-by":"crossref","first-page":"417","DOI":"10.1177\/000348948909800603","article-title":"Minor congenital laryngeal clefts: diagnosis and classification","volume":"98","author":"Benjamin","year":"1989","journal-title":"Ann Otol Rhinol Laryngol"},{"key":"10.1016\/j.prrv.2019.09.004_b0035","doi-asserted-by":"crossref","first-page":"1335","DOI":"10.1001\/archotol.132.12.1335","article-title":"The presentation and management of laryngeal cleft: a 10-year experience","volume":"132","author":"Rahbar","year":"2006","journal-title":"Arch Otolaryngol Head Neck Surg"},{"key":"10.1016\/j.prrv.2019.09.004_b0040","doi-asserted-by":"crossref","first-page":"227","DOI":"10.1016\/j.ijporl.2013.10.068","article-title":"Endoscopic repair of laryngotracheoesophageal clefts: experience in 17 cases","volume":"78","author":"Leishman","year":"2014","journal-title":"Int J Pediatr Otorhinolaryngol"},{"key":"10.1016\/j.prrv.2019.09.004_b0045","doi-asserted-by":"crossref","first-page":"905","DOI":"10.1016\/j.ijporl.2014.03.015","article-title":"Laryngeal cleft: evaluation and management","volume":"78","author":"Johnston","year":"2014","journal-title":"Int J Pediatr Otorhinolaryngol"},{"key":"10.1016\/j.prrv.2019.09.004_b0050","doi-asserted-by":"crossref","first-page":"98","DOI":"10.1136\/adc.72.1.98-c","article-title":"Familial occurrence of congenital laryngeal clefts","volume":"72","author":"Phelan","year":"1995","journal-title":"Arch Dis Child"},{"key":"10.1016\/j.prrv.2019.09.004_b0055","doi-asserted-by":"crossref","first-page":"12","DOI":"10.1136\/adc.29.143.12","article-title":"Non-inflammatory laryngeal stridor in infants","volume":"29","author":"Crooks","year":"1954","journal-title":"Arch Dis Child"},{"key":"10.1016\/j.prrv.2019.09.004_b0060","first-page":"525","article-title":"Failure of separation of larynx and trachea from the esophagus: persistent esophagotrachea","volume":"49","author":"Zachary","year":"1961","journal-title":"Surgery"},{"key":"10.1016\/j.prrv.2019.09.004_b0065","doi-asserted-by":"crossref","first-page":"275","DOI":"10.1136\/adc.48.4.275","article-title":"Familial occurrence of congenital laryngeal clefts","volume":"48","author":"Phelan","year":"1973","journal-title":"Arch Dis Child"},{"key":"10.1016\/j.prrv.2019.09.004_b0070","doi-asserted-by":"crossref","first-page":"706","DOI":"10.1111\/j.1365-2044.1984.tb06482.x","article-title":"Laryngotracheo-oesophageal cleft. A report of three cases","volume":"39","author":"Armitage","year":"1984","journal-title":"Anaesthesia"},{"key":"10.1016\/j.prrv.2019.09.004_b0075","doi-asserted-by":"crossref","first-page":"556","DOI":"10.1007\/BF01371899","article-title":"Cardiovascular malformations in rat fetuses with oesophageal atresia and tracheo-oesophageal fistula induced by adriamycin","volume":"12","author":"Qi BQ","year":"1997","journal-title":"Pediatr Surg Int"},{"key":"10.1016\/j.prrv.2019.09.004_b0080","doi-asserted-by":"crossref","first-page":"11","DOI":"10.1007\/s003830050501","article-title":"Visceral anomalies in prenatally adriamycin-exposed rat fetuses: a model for the VATER association","volume":"15","author":"Merei","year":"1999","journal-title":"Pediatr Surg Int"},{"key":"10.1016\/j.prrv.2019.09.004_b0085","doi-asserted-by":"crossref","first-page":"969","DOI":"10.1001\/archotol.2013.109","article-title":"Characterization of the larynx in ephrin-B2 knockout mice: a novel animal model for laryngeal clefts","volume":"138","author":"Neilan","year":"2012","journal-title":"Arch Otolaryngol Head Neck Surg"},{"key":"10.1016\/j.prrv.2019.09.004_b0090","doi-asserted-by":"crossref","first-page":"157","DOI":"10.1136\/jmg.25.3.157","article-title":"Further delineation of the G syndrome: a manageable genetic cause of infantile dysphagia","volume":"25","author":"Wilson","year":"1988","journal-title":"J Med Genet"},{"key":"10.1016\/j.prrv.2019.09.004_b0095","doi-asserted-by":"crossref","first-page":"59","DOI":"10.1002\/ajmg.1320030111","article-title":"The G syndrome: a case report","volume":"3","author":"Greenberg","year":"1979","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.prrv.2019.09.004_b0100","doi-asserted-by":"crossref","first-page":"185","DOI":"10.1177\/000348948909800304","article-title":"G syndrome and its otolaryngologic manifestations","volume":"98","author":"Howell","year":"1989","journal-title":"Ann Otol Rhinol Laryngol"},{"key":"10.1016\/j.prrv.2019.09.004_b0105","first-page":"505","article-title":"The G syndrome","volume":"121","author":"Little","year":"1971","journal-title":"Am. J. Dis. Child."},{"key":"10.1016\/j.prrv.2019.09.004_b0110","first-page":"54","article-title":"Two new familial cases of the G syndrome","volume":"11","author":"Frias","year":"1975","journal-title":"Birth Defects Original Article Series"},{"key":"10.1016\/j.prrv.2019.09.004_b0115","doi-asserted-by":"crossref","first-page":"131","DOI":"10.1002\/ajmg.1320020204","article-title":"The G and BBB syndromes: case presentations, genetics, and nosology","volume":"2","author":"Funderburk","year":"1978","journal-title":"Am J Med Genet."},{"key":"10.1016\/j.prrv.2019.09.004_b0120","doi-asserted-by":"crossref","first-page":"637","DOI":"10.1002\/ajmg.1320310319","article-title":"G syndrome: an unusual family","volume":"31","author":"Allanson","year":"1988","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.prrv.2019.09.004_b0125","doi-asserted-by":"crossref","first-page":"313","DOI":"10.1002\/ajmg.1320340303","article-title":"BBBG syndrome or Opitz syndrome: new family","volume":"34","author":"Verloes","year":"1989","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.prrv.2019.09.004_b0130","doi-asserted-by":"crossref","first-page":"303","DOI":"10.1007\/s00439-002-0892-2","article-title":"Human genetic disease caused by de novo mitochondrial-nuclear DNA transfer","volume":"112","author":"Turner","year":"2003","journal-title":"Hum Genet"},{"key":"10.1016\/j.prrv.2019.09.004_b0135","doi-asserted-by":"crossref","first-page":"885","DOI":"10.1101\/gr.227202","article-title":"Pattern of organization of human mitochondrial pseudogenes in the nuclear genome","volume":"12","author":"Woischnik","year":"2002","journal-title":"Genome Res"},{"key":"10.1016\/j.prrv.2019.09.004_b0140","doi-asserted-by":"crossref","first-page":"64","DOI":"10.1002\/1096-8628(20000904)94:1<64::AID-AJMG13>3.0.CO;2-D","article-title":"Asymptomatic laryngeal malformations are common in patients with Pallister-Hall syndrome","volume":"94","author":"Frank Ondrey","year":"2000","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.prrv.2019.09.004_b0145","doi-asserted-by":"crossref","first-page":"47","DOI":"10.1002\/ajmg.1320070110","article-title":"Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus and postaxial polydactyly\u2013a new syndrome? Part I: clinical, causal, and pathogenetic considerations","volume":"7","author":"Hall","year":"1980","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.prrv.2019.09.004_b0150","doi-asserted-by":"crossref","first-page":"232","DOI":"10.1111\/j.1399-0004.2009.01334.x","article-title":"Death in CHARGE syndrome after the neonatal period","volume":"77","author":"Bergman","year":"2010","journal-title":"Clin Genet"},{"key":"10.1016\/j.prrv.2019.09.004_b0155","doi-asserted-by":"crossref","first-page":"582","DOI":"10.1111\/j.1365-2044.1991.tb09664.x","article-title":"Incidence and management of airway problems in the CHARGE Association","volume":"46","author":"Stack","year":"1991","journal-title":"Anaesthesia"},{"key":"10.1016\/j.prrv.2019.09.004_b0160","doi-asserted-by":"crossref","first-page":"469","DOI":"10.1002\/lary.24804","article-title":"The association between laryngeal cleft and tracheoesophageal fistula: myth or reality?","volume":"125","author":"Fraga","year":"2015","journal-title":"Laryngoscope"},{"key":"10.1016\/j.prrv.2019.09.004_b0165","doi-asserted-by":"crossref","first-page":"28","DOI":"10.1034\/j.1399-0004.2000.580105.x","article-title":"Overlap of PIV syndrome, VACTERL and Pallister-Hall syndrome: clinical and molecular analysis","volume":"58","author":"Killoran","year":"2000","journal-title":"Clin Genet"},{"key":"10.1016\/j.prrv.2019.09.004_b0170","doi-asserted-by":"crossref","first-page":"306","DOI":"10.1002\/ajmg.c.31376","article-title":"Understanding the basis of auriculocondylar syndrome: Insights from human, mouse and zebrafish genetic studies","volume":"163C","author":"Clouthier","year":"2013","journal-title":"Am J Med Genet Part C, Semin Med Genet"},{"key":"10.1016\/j.prrv.2019.09.004_b0175","doi-asserted-by":"crossref","first-page":"174","DOI":"10.1136\/jmedgenet-2012-101331","article-title":"Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome","volume":"50","author":"Gordon","year":"2013","journal-title":"J Med Genet"},{"key":"10.1016\/j.prrv.2019.09.004_b0180","doi-asserted-by":"crossref","first-page":"156","DOI":"10.1097\/MCD.0000000000000006","article-title":"Chitayat-Hall syndrome: extending the clinical phenotype","volume":"22","author":"Rao","year":"2013","journal-title":"Clin Dysmorphol"},{"key":"10.1016\/j.prrv.2019.09.004_b0185","doi-asserted-by":"crossref","first-page":"837","DOI":"10.1177\/000348947908800619","article-title":"Laryngeal clefts: a histopathologic study and review","volume":"88","author":"Lim","year":"1979","journal-title":"Ann Otol Rhinol Laryngol"}],"container-title":["Paediatric Respiratory Reviews"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1526054219300855?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1526054219300855?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,26]],"date-time":"2025-10-26T19:34:27Z","timestamp":1761507267000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1526054219300855"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,2]]},"references-count":37,"alternative-id":["S1526054219300855"],"URL":"https:\/\/doi.org\/10.1016\/j.prrv.2019.09.004","relation":{},"ISSN":["1526-0542"],"issn-type":[{"type":"print","value":"1526-0542"}],"subject":[],"published":{"date-parts":[[2020,2]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Genetic factors in isolated and syndromic laryngeal cleft","name":"articletitle","label":"Article Title"},{"value":"Paediatric Respiratory Reviews","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.prrv.2019.09.004","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2019 Elsevier Ltd. All rights reserved.","name":"copyright","label":"Copyright"}]}}