{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,30]],"date-time":"2025-11-30T06:31:29Z","timestamp":1764484289460,"version":"3.46.0"},"reference-count":13,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2016,11,17]],"date-time":"2016-11-17T00:00:00Z","timestamp":1479340800000},"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":["Clinical Case Reports"],"published-print":{"date-parts":[[2017,1]]},"abstract":"<jats:title>Key Clinical Message<\/jats:title>\n                  <jats:p>We report two Japanese patients with Schinzel\u2013Giedion syndrome. When polyhydramnios is observed, additional fetal findings such as overlapping fingers, hydrocephalus, hydronephrosis, and very characteristic facial appearance comprising high, prominent forehead, hypertelorism, and depressed nasal root may suggest Schinzel\u2013Giedion syndrome.<\/jats:p>","DOI":"10.1002\/ccr3.738","type":"journal-article","created":{"date-parts":[[2016,11,17]],"date-time":"2016-11-17T03:42:33Z","timestamp":1479354153000},"page":"5-8","source":"Crossref","is-referenced-by-count":2,"title":["Genetic and prenatal findings in two Japanese patients with Schinzel\u2013Giedion syndrome"],"prefix":"10.1002","volume":"5","author":[{"given":"Nozomi","family":"Hishimura","sequence":"first","affiliation":[{"name":"Department of Pediatrics Tenshi Hospital N\u201012, E\u20103 Sapporo 065\u20108611 Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Michiko","family":"Watari","sequence":"additional","affiliation":[{"name":"Department of Obstetrics and Gynecology 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