{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T14:36:13Z","timestamp":1786977373669,"version":"build-2736575974"},"reference-count":12,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2023,2,19]],"date-time":"2023-02-19T00:00:00Z","timestamp":1676764800000},"content-version":"vor","delay-in-days":18,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Clinical Case Reports"],"published-print":{"date-parts":[[2023,2]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Smith\u2010Lemli\u2010Opitz syndrome (SLOS) is a relatively common genetic cause of developmental delay and may only present in conjunction with 2,3 toe syndactyly. This case series illustrates a milder phenotype of SLOS, where the predominant findings are neurocognitive in the presence of 2,3 toe syndactyly.<\/jats:p>","DOI":"10.1002\/ccr3.6920","type":"journal-article","created":{"date-parts":[[2023,2,20]],"date-time":"2023-02-20T00:24:27Z","timestamp":1676852667000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":3,"title":["Keeping you on your toes:\n                    <scp>Smith\u2013Lemli\u2013Opitz<\/scp>\n                    Syndrome is\u00a0an easily missed cause of developmental delays"],"prefix":"10.1002","volume":"11","author":[{"given":"Simone","family":"Coupe","sequence":"first","affiliation":[{"name":"NSW Biochemical Genetics Service The Children's Hospital at Westmead  Westmead New South Wales Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ashley","family":"Hertzog","sequence":"additional","affiliation":[{"name":"NSW Biochemical Genetics Service The Children's Hospital at Westmead  Westmead New South Wales Australia"},{"name":"Faculty of Medicine and Health University of Sydney  Westmead New South Wales Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2507-9961","authenticated-orcid":false,"given":"Carolyn","family":"Foran","sequence":"additional","affiliation":[{"name":"NSW Biochemical Genetics Service The Children's Hospital at Westmead  Westmead New South Wales Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Adviye Ayper","family":"Tolun","sequence":"additional","affiliation":[{"name":"NSW Biochemical Genetics Service The Children's Hospital at Westmead  Westmead New South Wales Australia"},{"name":"Faculty of Medicine and Health University of Sydney  Westmead New South Wales Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Megan","family":"Suthern","sequence":"additional","affiliation":[{"name":"Paediatric Department Wagga Wagga Base Hospital  Wagga Wagga New South Wales Australia"},{"name":"Rural Clinical School, Faculty of Medicine and Health University of New South Wales  Wagga Wagga New South Wales Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Clara W. 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