{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,31]],"date-time":"2026-08-31T13:42:55Z","timestamp":1788183775575,"version":"build-2803163510"},"reference-count":11,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2005,6,5]],"date-time":"2005-06-05T00:00:00Z","timestamp":1117929600000},"content-version":"vor","delay-in-days":6091,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1988,10]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>A 34\u2010week stillborn infant had omphalocele, agenesis of the sternum and anterior rib cage, membranous diaphragms with eventration of the viscera, ectopia cordis with absence of the pericardium, and congenital heart defect. These findings are consistent with a diagnosis of Cantrell pentalogy. The presence of bilateral clubfeet, spina bifida, hydrocephalus, abnormal ears, and horseshoe kidneys suggested a chromosome abnormality. Chromosome analysis showed trisomy 18. Individuals with manifestations of Cantrell pentalogy deserve cytogenetic evaluation.<\/jats:p>","DOI":"10.1002\/ajmg.1320310218","type":"journal-article","created":{"date-parts":[[2005,6,12]],"date-time":"2005-06-12T03:19:17Z","timestamp":1118546357000},"page":"391-394","source":"Crossref","is-referenced-by-count":35,"title":["Trisomy 18 with Cantrell pentalogy in a stillborn infant"],"prefix":"10.1002","volume":"31","author":[{"given":"Joyce E.","family":"Fox","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Elizabeth S.","family":"Gloster","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Raksha","family":"Mirchandani","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"John M.","family":"Opitz","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"James F.","family":"Reynolds","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2005,6,5]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.7863\/jum.1984.3.11.525"},{"key":"e_1_2_1_3_1","first-page":"602","article-title":"A syndrome of congenital defects involving the abdominal wall, sternum, diaphragm, pericardium, and heart","volume":"107","author":"Cantrell JR","year":"1958","journal-title":"Surg Gynecol Obstet"},{"key":"e_1_2_1_4_1","doi-asserted-by":"crossref","first-page":"218","DOI":"10.1542\/peds.62.2.218","article-title":"Thoracoabdominal ectopia cordis with mosaic Turner's syndrome: Report of a case","volume":"62","author":"Garson A","year":"1978","journal-title":"Pediatrics"},{"key":"e_1_2_1_5_1","doi-asserted-by":"crossref","first-page":"328","DOI":"10.1542\/peds.66.2.328a","article-title":"Ectopia cordis and chromosome errors","volume":"66","author":"King CR","year":"1980","journal-title":"Pediatrics"},{"key":"e_1_2_1_6_1","first-page":"523","article-title":"Ultrasonic diagnosis of ectopia cordis","volume":"61","author":"Mercer LJ","year":"1983","journal-title":"Obstet Gynecol"},{"key":"e_1_2_1_7_1","doi-asserted-by":"publisher","DOI":"10.1016\/0002-8703(78)90484-2"},{"key":"e_1_2_1_8_1","doi-asserted-by":"publisher","DOI":"10.1002\/pd.1970040607"},{"key":"e_1_2_1_9_1","doi-asserted-by":"publisher","DOI":"10.3109\/15513818609068872"},{"key":"e_1_2_1_10_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-3476(82)80261-8"},{"key":"e_1_2_1_11_1","doi-asserted-by":"publisher","DOI":"10.3109\/14017438309099351"},{"key":"e_1_2_1_12_1","first-page":"778","article-title":"Combined congenital defects of the anterior abdominal wall, sternum, diaphragm, pericardium, and heart: A case report and review of the syndrome","volume":"50","author":"Toyama WM","year":"1972","journal-title":"Pediatrics"}],"container-title":["American Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.1320310218","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.1320310218","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,21]],"date-time":"2023-10-21T04:04:03Z","timestamp":1697861043000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajmg.1320310218"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1988,10]]},"references-count":11,"journal-issue":{"issue":"2","published-print":{"date-parts":[[1988,10]]}},"alternative-id":["10.1002\/ajmg.1320310218"],"URL":"https:\/\/doi.org\/10.1002\/ajmg.1320310218","archive":["Portico"],"relation":{},"ISSN":["0148-7299","1096-8628"],"issn-type":[{"value":"0148-7299","type":"print"},{"value":"1096-8628","type":"electronic"}],"subject":[],"published":{"date-parts":[[1988,10]]}}}