{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,23]],"date-time":"2026-01-23T10:04:54Z","timestamp":1769162694233,"version":"3.49.0"},"reference-count":7,"publisher":"Elsevier BV","issue":"4","license":[{"start":{"date-parts":[[2019,4,1]],"date-time":"2019-04-01T00:00:00Z","timestamp":1554076800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2019,1,16]],"date-time":"2019-01-16T00:00:00Z","timestamp":1547596800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Radiology Case Reports"],"published-print":{"date-parts":[[2019,4]]},"DOI":"10.1016\/j.radcr.2019.01.003","type":"journal-article","created":{"date-parts":[[2019,1,27]],"date-time":"2019-01-27T10:57:10Z","timestamp":1548586630000},"page":"448-451","source":"Crossref","is-referenced-by-count":4,"title":["Radiography of Chitayat syndrome in an infant male"],"prefix":"10.1016","volume":"14","author":[{"given":"Seong Hwan","family":"Shin","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Emma","family":"StJoseph","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Khalid","family":"Mannan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Khalid","family":"Khan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"1","key":"10.1016\/j.radcr.2019.01.003_bib0001","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1002\/ajmg.1320450103","article-title":"Hyperphalangism, facial anomalies, hallux valgus, and bronchomalacia: a new syndrome?","volume":"45","author":"Chitayat","year":"1993","journal-title":"Am J Med Genet"},{"issue":"3","key":"10.1016\/j.radcr.2019.01.003_bib0002","doi-asserted-by":"crossref","first-page":"157","DOI":"10.1136\/jmedgenet-2016-104143","article-title":"Chitayat syndrome: hyperphalangism, characteristic facies, hallux valgus and bronchomalacia results from a recurrent c.266A\u202f>\u202fG p.(Tyr89Cys) variant in the ERF gene","volume":"54","author":"Balasubramanian","year":"2016","journal-title":"J Med Genet"},{"issue":"188","key":"10.1016\/j.radcr.2019.01.003_bib0003","doi-asserted-by":"crossref","first-page":"461","DOI":"10.1136\/adc.36.188.461-a","article-title":"Differential diagnose von Krankheitssymptomen bei Kindern und Jugendlichen","volume":"36","author":"Catel","year":"1961","journal-title":"Arch Dis Childhood"},{"issue":"5","key":"10.1016\/j.radcr.2019.01.003_bib0004","doi-asserted-by":"crossref","first-page":"452","DOI":"10.1016\/j.ejmg.2008.03.005","article-title":"Catel\u2013Manzke syndrome: two new patients and a critical review of the literature","volume":"51","author":"Manzke","year":"2008","journal-title":"Eur J Med Genet"},{"issue":"6","key":"10.1016\/j.radcr.2019.01.003_bib0005","doi-asserted-by":"crossref","first-page":"763","DOI":"10.1016\/j.ajhg.2014.11.004","article-title":"Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome","volume":"95","author":"Ehmke","year":"2014","journal-title":"Am J Hum Genet"},{"issue":"8","key":"10.1016\/j.radcr.2019.01.003_bib0006","doi-asserted-by":"crossref","first-page":"2056","DOI":"10.1002\/ajmg.a.36016","article-title":"A mother and daughter with a novel phenotype of hand and foot abnormalities and severe pectus excavatum","volume":"161","author":"Low","year":"2013","journal-title":"Am J Med Genet A"},{"issue":"6","key":"10.1016\/j.radcr.2019.01.003_bib0007","doi-asserted-by":"crossref","first-page":"757","DOI":"10.1016\/j.ajhg.2010.10.003","article-title":"Temtamy preaxial brachydactyly syndrome is caused by loss-of-function mutations in chondroitin synthase 1, a potential target of BMP signaling","volume":"87","author":"Li","year":"2010","journal-title":"Am J Hum Genet"}],"container-title":["Radiology Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1930043318304801?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1930043318304801?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,3,12]],"date-time":"2019-03-12T00:02:53Z","timestamp":1552348973000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1930043318304801"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,4]]},"references-count":7,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2019,4]]}},"alternative-id":["S1930043318304801"],"URL":"https:\/\/doi.org\/10.1016\/j.radcr.2019.01.003","relation":{},"ISSN":["1930-0433"],"issn-type":[{"value":"1930-0433","type":"print"}],"subject":[],"published":{"date-parts":[[2019,4]]}}}