{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T20:46:42Z","timestamp":1760906802920,"version":"build-2065373602"},"reference-count":26,"publisher":"BMJ","issue":"8","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Med Genet"],"published-print":{"date-parts":[[2001,8,1]]},"DOI":"10.1136\/jmg.38.8.556","type":"journal-article","created":{"date-parts":[[2002,7,27]],"date-time":"2002-07-27T06:34:46Z","timestamp":1027751686000},"page":"556-558","source":"Crossref","is-referenced-by-count":8,"title":["Congenital diaphragmatic hernia and interstitial deletion of chromosome 3"],"prefix":"10.1136","volume":"38","author":[{"given":"P","family":"Brennan","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G D","family":"Croaker","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M","family":"Heath","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[2001,8,1]]},"reference":[{"key":"2025101800521736000_38.8.556.1","doi-asserted-by":"publisher","DOI":"10.1016\/S0009-9260(05)81015-3"},{"key":"2025101800521736000_38.8.556.2","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.17.2.135"},{"key":"2025101800521736000_38.8.556.3","doi-asserted-by":"publisher","DOI":"10.1136\/adc.69.1_Spec_No.68"},{"key":"2025101800521736000_38.8.556.4","doi-asserted-by":"crossref","first-page":"187","DOI":"10.1002\/pd.1970140308","article-title":"Prenatal diagnosis of congenital diaphragmatic hernia: a retrospective analysis of 28 cases.","volume":"14","author":"Manni","year":"1994","journal-title":"Prenat Diagn"},{"key":"2025101800521736000_38.8.556.5","doi-asserted-by":"crossref","first-page":"21","DOI":"10.1159\/000263386","article-title":"Prenatal diagnosis of congenital diaphragmatic hernia: associated malformations and chromosome defects.","volume":"4","author":"Thorpe-Beeston","year":"1989","journal-title":"Fetal Ther"},{"key":"2025101800521736000_38.8.556.6","doi-asserted-by":"publisher","DOI":"10.1002\/(SICI)1097-0223(199611)16:11<1003::AID-PD995>3.0.CO;2-D"},{"key":"2025101800521736000_38.8.556.7","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.31.9.735"},{"key":"2025101800521736000_38.8.556.8","doi-asserted-by":"crossref","first-page":"781","DOI":"10.1002\/ajmg.1320270406","article-title":"Interstitial deletion of the long arm of chromosome 3: case report, review, and definition of a phenotype.","volume":"27","author":"Alvarado","year":"1987","journal-title":"Am J Med Genet"},{"key":"2025101800521736000_38.8.556.9","doi-asserted-by":"publisher","DOI":"10.1006\/geno.1998.5512"},{"key":"2025101800521736000_38.8.556.10","first-page":"42","article-title":"Deletion of the proximal long arm of chromosome 3 in an infant with features of Turner syndrome.","volume":"28","author":"Jenkins","year":"1985","journal-title":"Ann Genet"},{"key":"2025101800521736000_38.8.556.11","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.24.5.305"},{"key":"2025101800521736000_38.8.556.12","first-page":"1","article-title":"A case report of partial deletion of the long arm of the no 3 chromosome.","volume":"4","author":"Arai","year":"1982","journal-title":"Med Genet Res"},{"key":"2025101800521736000_38.8.556.13","doi-asserted-by":"crossref","first-page":"220","DOI":"10.1111\/j.1399-0004.1998.tb02681.x","article-title":"Deletion of chromosome 3q proximal region gives rise to a variable phenotype.","volume":"53","author":"Ogilvie","year":"1998","journal-title":"Clin Genet"},{"key":"2025101800521736000_38.8.556.14","first-page":"A124","article-title":"A new interstitial deletion of the long arm of chromosome 3.","volume":"39","author":"McMorrow","year":"1986","journal-title":"Am J Hum Genet"},{"key":"2025101800521736000_38.8.556.15","doi-asserted-by":"crossref","first-page":"292","DOI":"10.1097\/00019605-199410000-00003","article-title":"A new case of interstitial deletion of chromosome 3q, del(3q)(q13.12q21.3), with agenesis of the corpus callosum.","volume":"3","author":"Genuardi","year":"1994","journal-title":"Clin Dysmorphol"},{"key":"2025101800521736000_38.8.556.16","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.31.8.647"},{"key":"2025101800521736000_38.8.556.17","doi-asserted-by":"crossref","first-page":"267","DOI":"10.1007\/BF00291674","article-title":"Association of a new chromosomal deletion [del(1)(q32q42)] with diaphragmatic hernia: assignment of a human ferritin gene.","volume":"78","author":"Youssoufian","year":"1988","journal-title":"Hum Genet"},{"key":"2025101800521736000_38.8.556.18","doi-asserted-by":"crossref","first-page":"1055","DOI":"10.1002\/(SICI)1097-0223(1998100)18:10<1055::AID-PD405>3.0.CO;2-I","article-title":"Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literature.","volume":"18","author":"Faivre","year":"1998","journal-title":"Prenat Diagn"},{"key":"2025101800521736000_38.8.556.19","doi-asserted-by":"crossref","first-page":"52","DOI":"10.1159\/000264193","article-title":"Associated malformations and chromosome defects in congenital diaphragmatic hernia.","volume":"10","author":"Bollman","year":"1995","journal-title":"Fetal Diagn Ther"},{"key":"2025101800521736000_38.8.556.20","doi-asserted-by":"crossref","first-page":"787","DOI":"10.1002\/pd.1970140904","article-title":"Tetrasomy 12p (Pallister-Killian syndrome): ultrasound indicators and confirmation by interphase fish.","volume":"14","author":"Wilson","year":"1994","journal-title":"Prenat Diagn"},{"key":"2025101800521736000_38.8.556.21","doi-asserted-by":"publisher","DOI":"10.1002\/(SICI)1096-8628(20000117)90:2<120::AID-AJMG6>3.0.CO;2-R"},{"key":"2025101800521736000_38.8.556.22","doi-asserted-by":"crossref","first-page":"319","DOI":"10.1111\/j.1399-0004.1998.tb02706.x","article-title":"Two cases of prenatally diagnosed diaphragmatic hernia accompanied by the same undescribed chromosomal deletion (15q24 de novo).","volume":"53","author":"Bettelheim","year":"1998","journal-title":"Clin Genet"},{"key":"2025101800521736000_38.8.556.23","doi-asserted-by":"crossref","first-page":"287","DOI":"10.1097\/00019605-199410000-00002","article-title":"Severe microphthalmia, diaphragmatic hernia and Fallot's tetralogy associated with a chromosome 1;15 translocation.","volume":"3","author":"Smith","year":"1994","journal-title":"Clin Dysmorphol"},{"key":"2025101800521736000_38.8.556.24","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320470716"},{"key":"2025101800521736000_38.8.556.25","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.28.9.639"},{"key":"2025101800521736000_38.8.556.26","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.32.10.837"}],"container-title":["Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jmg.38.8.556","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,10,18]],"date-time":"2025-10-18T07:52:23Z","timestamp":1760773943000},"score":1,"resource":{"primary":{"URL":"https:\/\/jmg.bmj.com\/lookup\/doi\/10.1136\/jmg.38.8.556"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2001,8,1]]},"references-count":26,"journal-issue":{"issue":"8","published-online":{"date-parts":[[2001,8,1]]},"published-print":{"date-parts":[[2001,8,1]]}},"alternative-id":["10.1136\/jmg.38.8.556"],"URL":"https:\/\/doi.org\/10.1136\/jmg.38.8.556","relation":{},"ISSN":["0022-2593","1468-6244"],"issn-type":[{"type":"print","value":"0022-2593"},{"type":"electronic","value":"1468-6244"}],"subject":[],"published":{"date-parts":[[2001,8,1]]}}}