{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,14]],"date-time":"2026-02-14T09:32:49Z","timestamp":1771061569442,"version":"3.50.1"},"reference-count":16,"publisher":"Elsevier BV","issue":"2","license":[{"start":{"date-parts":[[2010,11,1]],"date-time":"2010-11-01T00:00:00Z","timestamp":1288569600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2010,11,1]],"date-time":"2010-11-01T00:00:00Z","timestamp":1288569600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2010,11,1]],"date-time":"2010-11-01T00:00:00Z","timestamp":1288569600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2010,11,1]],"date-time":"2010-11-01T00:00:00Z","timestamp":1288569600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2010,11,1]],"date-time":"2010-11-01T00:00:00Z","timestamp":1288569600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2010,11,1]],"date-time":"2010-11-01T00:00:00Z","timestamp":1288569600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2010,11,1]],"date-time":"2010-11-01T00:00:00Z","timestamp":1288569600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","internationaljournalofcardiology.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["International Journal of Cardiology"],"published-print":{"date-parts":[[2010,11]]},"DOI":"10.1016\/j.ijcard.2009.05.067","type":"journal-article","created":{"date-parts":[[2009,7,20]],"date-time":"2009-07-20T04:11:08Z","timestamp":1248063068000},"page":"224-226","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":11,"title":["Genetic variation of SAL-Like 4 (SALL4) in ventricular septal defect"],"prefix":"10.1016","volume":"145","author":[{"given":"Binbin","family":"Wang","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lin","family":"Li","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xiaodong","family":"Xie","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jing","family":"Wang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jinting","family":"Yan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yuan","family":"Mu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xu","family":"Ma","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.ijcard.2009.05.067_bb0005","doi-asserted-by":"crossref","first-page":"1890","DOI":"10.1016\/S0735-1097(02)01886-7","article-title":"The incidence of congenital heart disease","volume":"39","author":"Hoffman","year":"2002","journal-title":"J Am Coll Cardiol"},{"key":"10.1016\/j.ijcard.2009.05.067_bb0010","doi-asserted-by":"crossref","first-page":"270","DOI":"10.1038\/nature03940","article-title":"Mutations in NOTCH1 cause aortic valve disease","volume":"437","author":"Garg","year":"2005","journal-title":"Nature"},{"key":"10.1016\/j.ijcard.2009.05.067_bb0015","doi-asserted-by":"crossref","first-page":"108","DOI":"10.1126\/science.281.5373.108","article-title":"Congenital heart disease caused by mutations in the transcription factor NKX2-5","volume":"281","author":"Schott","year":"1998","journal-title":"Science"},{"key":"10.1016\/j.ijcard.2009.05.067_bb0020","doi-asserted-by":"crossref","first-page":"163","DOI":"10.1093\/hmg\/10.2.163","article-title":"Familial Tetralogy of Fallot caused by mutation in the jagged1 gene","volume":"10","author":"Eldadah","year":"2001","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.ijcard.2009.05.067_bb0025","doi-asserted-by":"crossref","first-page":"443","DOI":"10.1038\/nature01827","article-title":"GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5","volume":"424","author":"Garg","year":"2003","journal-title":"Nature"},{"key":"10.1016\/j.ijcard.2009.05.067_bb0030","doi-asserted-by":"crossref","first-page":"10","DOI":"10.1196\/annals.1420.003","article-title":"Genetic mechanisms controlling cardiovascular development","volume":"1123","author":"Bentham","year":"2008","journal-title":"Ann NY Acad Sci"},{"key":"10.1016\/j.ijcard.2009.05.067_bb0035","doi-asserted-by":"crossref","first-page":"2919","DOI":"10.1073\/pnas.96.6.2919","article-title":"Different TBX5 interactions in heart and limb defined by Holt\u2013Oram syndrome mutations","volume":"96","author":"Basson","year":"1999","journal-title":"P Nalt Acad Sci USA"},{"key":"10.1016\/j.ijcard.2009.05.067_bb0040","doi-asserted-by":"crossref","first-page":"211","DOI":"10.1097\/00001573-200405000-00004","article-title":"TBX5 mutations and congenital heart disease: Holt\u2013Oram syndrome revealed","volume":"19","author":"Mori","year":"2004","journal-title":"Curr Opin Cardiol"},{"key":"10.1016\/j.ijcard.2009.05.067_bb0045","doi-asserted-by":"crossref","first-page":"176","DOI":"10.1002\/humu.20215","article-title":"SALL4 mutations in Okihiro syndrome (Duane-radial ray syndrome), acro-renal-ocular syndrome, and related disorders","volume":"26","author":"Kohlhase","year":"2005","journal-title":"Hum Mutat"},{"key":"10.1016\/j.ijcard.2009.05.067_bb0050","doi-asserted-by":"crossref","first-page":"2979","DOI":"10.1093\/hmg\/11.23.2979","article-title":"Okihiro syndrome is caused by SALL4 mutations","volume":"11","author":"Kohlhase","year":"2002","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.ijcard.2009.05.067_bb0055","doi-asserted-by":"crossref","first-page":"473","DOI":"10.1136\/jmg.40.7.473","article-title":"Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt\u2013Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy","volume":"40","author":"Kohlhase","year":"2003","journal-title":"J Med Genet"},{"key":"10.1016\/j.ijcard.2009.05.067_bb0060","doi-asserted-by":"crossref","first-page":"e102","DOI":"10.1136\/jmg.2004.019505","article-title":"Novel mutations in the gene SALL4 provide further evidence for acro-renal-ocular and Okihiro syndromes being allelic entities, and extend the phenotypic spectrum","volume":"41","author":"Borozdin","year":"2004","journal-title":"J Med Genet"},{"key":"10.1016\/j.ijcard.2009.05.067_bb0065","doi-asserted-by":"crossref","first-page":"175","DOI":"10.1038\/ng1707","article-title":"Cooperative and antagonistic interactions between Sall4 and Tbx5 pattern the mouse limb and heart","volume":"38","author":"Koshiba-Takeuchi","year":"2006","journal-title":"Nat Genet"},{"key":"10.1016\/j.ijcard.2009.05.067_bb0070","doi-asserted-by":"crossref","first-page":"3005","DOI":"10.1242\/dev.02457","article-title":"The murine homolog of SALL4, a causative gene in Okihiro syndrome, is essential for embryonic stem cell proliferation, and cooperates with Sall1 in anorectal, heart, brain and kidney development","volume":"133","author":"Sakaki-Yumoto","year":"2006","journal-title":"Development"},{"key":"10.1016\/j.ijcard.2009.05.067_bb0075","doi-asserted-by":"crossref","first-page":"285","DOI":"10.1016\/j.ydbio.2006.02.009","article-title":"The vertebrate spalt genes in development and disease","volume":"293","author":"Sweetman","year":"2006","journal-title":"Dev Biol"},{"key":"10.1016\/j.ijcard.2009.05.067_bb0080","doi-asserted-by":"crossref","first-page":"149","DOI":"10.1016\/j.ijcard.2008.11.048","article-title":"Ethical authorship and publishing","volume":"131","author":"Coats","year":"2009","journal-title":"Int J Cardiol"}],"container-title":["International Journal of Cardiology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0167527309006263?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0167527309006263?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,28]],"date-time":"2025-09-28T20:27:14Z","timestamp":1759091234000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0167527309006263"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2010,11]]},"references-count":16,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2010,11]]}},"alternative-id":["S0167527309006263"],"URL":"https:\/\/doi.org\/10.1016\/j.ijcard.2009.05.067","relation":{},"ISSN":["0167-5273"],"issn-type":[{"value":"0167-5273","type":"print"}],"subject":[],"published":{"date-parts":[[2010,11]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Genetic variation of SAL-Like 4 (SALL4) in ventricular septal defect","name":"articletitle","label":"Article Title"},{"value":"International Journal of Cardiology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ijcard.2009.05.067","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2009 Elsevier Ireland Ltd. All rights reserved.","name":"copyright","label":"Copyright"}]}}