{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T10:27:31Z","timestamp":1761733651067,"version":"build-2065373602"},"reference-count":9,"publisher":"Elsevier BV","issue":"6-7","license":[{"start":{"date-parts":[[2015,6,1]],"date-time":"2015-06-01T00:00:00Z","timestamp":1433116800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2015,6,1]],"date-time":"2015-06-01T00:00:00Z","timestamp":1433116800000},"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":["European Journal of Medical Genetics"],"published-print":{"date-parts":[[2015,6]]},"DOI":"10.1016\/j.ejmg.2015.04.002","type":"journal-article","created":{"date-parts":[[2015,4,20]],"date-time":"2015-04-20T12:15:31Z","timestamp":1429532131000},"page":"336-340","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":2,"title":["De novo deletion of HOXB gene cluster in a patient with failure to thrive, developmental delay, gastroesophageal reflux and bronchiectasis"],"prefix":"10.1016","volume":"58","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-5435-0781","authenticated-orcid":false,"given":"Sander","family":"Pajusalu","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tiia","family":"Reimand","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Oivi","family":"Uibo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Maire","family":"Vasar","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Inga","family":"Talvik","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Olga","family":"Zilina","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Pille","family":"Tammur","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Katrin","family":"\u00d5unap","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.ejmg.2015.04.002_bib1","doi-asserted-by":"crossref","first-page":"843","DOI":"10.1093\/oxfordjournals.molbev.a025825","article-title":"Phylogenetic reconstruction of vertebrate Hox cluster duplications","volume":"14","author":"Bailey","year":"1997","journal-title":"Mol Biol Evol"},{"key":"10.1016\/j.ejmg.2015.04.002_bib2","doi-asserted-by":"crossref","first-page":"54","DOI":"10.1111\/j.1399-0004.1993.tb04452.x","article-title":"Interstitial deletion del(17) (q21.3q23 or 24.2) syndrome","volume":"43","author":"Dallapiccola","year":"1993","journal-title":"Clin Genet"},{"key":"10.1016\/j.ejmg.2015.04.002_bib3","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1093\/molehr\/3.2.115","article-title":"Developmental functions of mammalian Hox genes","volume":"3","author":"Favier","year":"1997","journal-title":"Mol Hum Reprod"},{"key":"10.1016\/j.ejmg.2015.04.002_bib4","doi-asserted-by":"crossref","first-page":"258","DOI":"10.1111\/j.1399-0004.1993.tb03893.x","article-title":"Additional case of de novo interstitial deletion del(17)(q21.3q23) and expansion of the phenotype","volume":"44","author":"Khalifa","year":"1993","journal-title":"Clin Genet"},{"key":"10.1016\/j.ejmg.2015.04.002_bib5","doi-asserted-by":"crossref","first-page":"71","DOI":"10.1006\/dbio.2000.9683","article-title":"A\u00a0large targeted deletion of Hoxb1-Hoxb9 produces a series of single-segment anterior homeotic transformations","volume":"222","author":"Medina-Martinez","year":"2000","journal-title":"Dev Biol"},{"key":"10.1016\/j.ejmg.2015.04.002_bib6","doi-asserted-by":"crossref","first-page":"54","DOI":"10.1111\/j.1399-0004.1992.tb03631.x","article-title":"A\u00a0unique de novo interstitial deletion del(17)(q21.3q23) in a phenotypically abnormal infant","volume":"41","author":"Park","year":"1992","journal-title":"Clin Genet"},{"key":"10.1016\/j.ejmg.2015.04.002_bib7","doi-asserted-by":"crossref","first-page":"490","DOI":"10.1038\/nature13723","article-title":"A\u00a0Hox regulatory network of hindbrain segmentation is conserved to the base of vertebrates","volume":"514","author":"Parker","year":"2014","journal-title":"Nature"},{"key":"10.1016\/j.ejmg.2015.04.002_bib8","doi-asserted-by":"crossref","first-page":"74","DOI":"10.1016\/j.ejmg.2007.09.003","article-title":"A\u00a0580 kb microdeletion in 17q21.32 associated with mental retardation, microcephaly, cleft palate, and cardiac malformation","volume":"51","author":"Rooryck","year":"2008","journal-title":"Eur J Med Genet"},{"key":"10.1016\/j.ejmg.2015.04.002_bib9","doi-asserted-by":"crossref","first-page":"570","DOI":"10.1038\/sj.ejhg.5201795","article-title":"De novo t(12;17)(p13.3;q21.3) translocation with a breakpoint near the 5' end of the HOXB gene cluster in a patient with developmental delay and skeletal malformations","volume":"15","author":"Yue","year":"2007","journal-title":"Eur J Hum Genet"}],"container-title":["European Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1769721215000750?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1769721215000750?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T03:42:06Z","timestamp":1761709326000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1769721215000750"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,6]]},"references-count":9,"journal-issue":{"issue":"6-7","published-print":{"date-parts":[[2015,6]]}},"alternative-id":["S1769721215000750"],"URL":"https:\/\/doi.org\/10.1016\/j.ejmg.2015.04.002","relation":{},"ISSN":["1769-7212"],"issn-type":[{"type":"print","value":"1769-7212"}],"subject":[],"published":{"date-parts":[[2015,6]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"De novo deletion of HOXB gene cluster in a patient with failure to thrive, developmental delay, gastroesophageal reflux and bronchiectasis","name":"articletitle","label":"Article Title"},{"value":"European Journal of Medical Genetics","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ejmg.2015.04.002","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2015 Elsevier Masson SAS. All rights reserved.","name":"copyright","label":"Copyright"}]}}