{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T20:50:15Z","timestamp":1760907015076},"reference-count":14,"publisher":"Wiley","issue":"10","license":[{"start":{"date-parts":[[2016,8,19]],"date-time":"2016-08-19T00:00:00Z","timestamp":1471564800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["81370727"],"award-info":[{"award-number":["81370727"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Prenatal Diagnosis"],"published-print":{"date-parts":[[2016,10]]},"abstract":"<jats:p><jats:bold>What's Already Known About This Topic?<\/jats:bold>\n<jats:list list-type=\"bullet\">\n<jats:list-item><jats:p>Wolf\u2013Hirschhorn syndrome is a genetic disorder caused by partial deletion of the short arm of chromosome<\/jats:p><\/jats:list-item>\n<jats:list-item><jats:p>It consists of a broad spectrum of clinical manifestations. The deletion size also varies significantly.<\/jats:p><\/jats:list-item>\n<\/jats:list><\/jats:p><jats:p><jats:bold>What Does This Study Add?<\/jats:bold>\n<jats:list list-type=\"bullet\">\n<jats:list-item><jats:p>This study found that a non\u2010coding RNA (NR_130734) might be involved in cardiovascular development by analyzing the genotype\u2013phenotype correlation of two fetuses with Wolf\u2013Hirschhorn syndrome.<\/jats:p><\/jats:list-item>\n<\/jats:list><\/jats:p>","DOI":"10.1002\/pd.4884","type":"journal-article","created":{"date-parts":[[2016,8,8]],"date-time":"2016-08-08T18:31:15Z","timestamp":1470681075000},"page":"979-981","source":"Crossref","is-referenced-by-count":1,"title":["A genotype\u2013phenotype correlation study reveals that a non\u2010coding RNA might be associated with cardiovascular anomalies in fetuses with WHS"],"prefix":"10.1002","volume":"36","author":[{"given":"Yi","family":"Wu","sequence":"first","affiliation":[{"name":"Prenatal Diagnosis Center, International Peace Maternal &amp; 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