{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T10:27:54Z","timestamp":1761733674695,"version":"build-2065373602"},"reference-count":8,"publisher":"Elsevier BV","issue":"4","license":[{"start":{"date-parts":[[2015,4,1]],"date-time":"2015-04-01T00:00:00Z","timestamp":1427846400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2015,4,1]],"date-time":"2015-04-01T00:00:00Z","timestamp":1427846400000},"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":[[2015,4]]},"DOI":"10.1016\/j.ejmg.2015.02.007","type":"journal-article","created":{"date-parts":[[2015,2,25]],"date-time":"2015-02-25T19:47:19Z","timestamp":1424893639000},"page":"203-204","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":5,"title":["Facioscapulohumeral muscular dystrophy as a genetic cause of pectus excavatum"],"prefix":"10.1016","volume":"58","author":[{"given":"Karlien","family":"Mul","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"George W.","family":"Padberg","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nicol C.","family":"Voermans","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.ejmg.2015.02.007_bib1","doi-asserted-by":"crossref","first-page":"414","DOI":"10.1016\/j.ejmg.2014.04.017","article-title":"Pectus excavatum and carinatum","volume":"57","author":"Cobben","year":"2014","journal-title":"Eur J Med Genet"},{"year":"2013","series-title":"Smith's Recognizable Patterns of Human Malformation","author":"Jones","key":"10.1016\/j.ejmg.2015.02.007_bib2"},{"key":"10.1016\/j.ejmg.2015.02.007_bib3","doi-asserted-by":"crossref","first-page":"1056","DOI":"10.1212\/WNL.0000000000000797","article-title":"Population-based incidence and prevalence of facioscapulohumeral dystrophy","volume":"83","author":"Deenen","year":"2014","journal-title":"Neurology"},{"key":"10.1016\/j.ejmg.2015.02.007_bib4","doi-asserted-by":"crossref","first-page":"2004","DOI":"10.1016\/j.jpedsurg.2009.07.029","article-title":"Etiology of chest wall deformities\u2013a genetic review for the treating physician","volume":"44","author":"Kotzot","year":"2009","journal-title":"J Pediatr Surg"},{"key":"10.1016\/j.ejmg.2015.02.007_bib5","doi-asserted-by":"crossref","first-page":"512","DOI":"10.1016\/j.mehy.2014.01.023","article-title":"Irregular location of major pectoral muscle can be a causative factor of pectus excavatum","volume":"82","author":"Nagasao","year":"2014","journal-title":"Med Hypotheses"},{"year":"1982","series-title":"Facioscapulohumeral Disease","author":"Padberg","key":"10.1016\/j.ejmg.2015.02.007_bib6"},{"year":"1983","series-title":"De ziekte van Landouzy-Dejerine. Een computer-tomografische studie van de skeletmusculatuur","author":"Patijn","key":"10.1016\/j.ejmg.2015.02.007_bib7"},{"key":"10.1016\/j.ejmg.2015.02.007_bib8","doi-asserted-by":"crossref","first-page":"176","DOI":"10.1212\/01.WNL.0000133126.86377.E8","article-title":"Ventilatory support in facioscapulohumeral muscular dystrophy","volume":"63","author":"Wohlgemuth","year":"2004","journal-title":"Neurology"}],"container-title":["European Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1769721215000397?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1769721215000397?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T03:41:46Z","timestamp":1761709306000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1769721215000397"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,4]]},"references-count":8,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2015,4]]}},"alternative-id":["S1769721215000397"],"URL":"https:\/\/doi.org\/10.1016\/j.ejmg.2015.02.007","relation":{},"ISSN":["1769-7212"],"issn-type":[{"type":"print","value":"1769-7212"}],"subject":[],"published":{"date-parts":[[2015,4]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Facioscapulohumeral muscular dystrophy as a genetic cause of pectus excavatum","name":"articletitle","label":"Article Title"},{"value":"European Journal of Medical Genetics","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ejmg.2015.02.007","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"simple-article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2015 Elsevier Masson SAS. All rights reserved.","name":"copyright","label":"Copyright"}]}}