{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,16]],"date-time":"2026-10-16T12:02:43Z","timestamp":1792152163561,"version":"4.4.0"},"reference-count":6,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2005,11,21]],"date-time":"2005-11-21T00:00:00Z","timestamp":1132531200000},"content-version":"vor","delay-in-days":7935,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Prenatal Diagnosis"],"published-print":{"date-parts":[[1984,3]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Chondroectodermal dysplasia (Ellis\u2010van Creveld syndrome) has previously been diagnosed prenatally only once, using fetoscopy. We report on two consecutive pregnancies in a woman at risk of having a child with the syndrome during which fetoscopic visualization was performed. Ellis\u2010van Creveld syndrome was diagnosed prenatally in one instance, while it could be excluded in the other one. Non\u2010invasive prenatal diagnosis of the syndrome is discussed.<\/jats:p>","DOI":"10.1002\/pd.1970040212","type":"journal-article","created":{"date-parts":[[2007,3,3]],"date-time":"2007-03-03T18:05:49Z","timestamp":1172945149000},"page":"155-159","source":"Crossref","is-referenced-by-count":17,"title":["Prenatal diagnosis of chondroectodermal dysplasia with fetoscopy"],"prefix":"10.1002","volume":"4","author":[{"given":"The\u2010Hung","family":"Bui","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lars","family":"Marsk","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ole","family":"Ekl\u00f6f","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Klas","family":"Theorell","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2005,11,21]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1016\/0002-9378(82)90735-9"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1056\/NEJM197708042970507"},{"key":"e_1_2_1_4_1","first-page":"489","volume-title":"Mendelian Inheritance in Man","author":"McKusick V. A.","year":"1978"},{"key":"e_1_2_1_5_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1471-0528.1980.tb04577.x"},{"key":"e_1_2_1_6_1","doi-asserted-by":"crossref","first-page":"29","DOI":"10.1177\/014107688007300107","article-title":"Value of fetoscopy in prenatal diagnosis","volume":"73","author":"Rodeck C. H.","year":"1980","journal-title":"J. Roy. Soc. Med."},{"key":"e_1_2_1_7_1","first-page":"393","article-title":"The genetics of hand malformations","volume":"14","author":"Temtamy S.","year":"1978","journal-title":"Birth Defects: Or. Art. Ser."}],"container-title":["Prenatal Diagnosis"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fpd.1970040212","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/obgyn.onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/pd.1970040212","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,19]],"date-time":"2023-10-19T21:45:07Z","timestamp":1697751907000},"score":1,"resource":{"primary":{"URL":"https:\/\/obgyn.onlinelibrary.wiley.com\/doi\/10.1002\/pd.1970040212"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1984,3]]},"references-count":6,"journal-issue":{"issue":"2","published-print":{"date-parts":[[1984,3]]}},"alternative-id":["10.1002\/pd.1970040212"],"URL":"https:\/\/doi.org\/10.1002\/pd.1970040212","archive":["Portico"],"relation":{},"ISSN":["0197-3851","1097-0223"],"issn-type":[{"value":"0197-3851","type":"print"},{"value":"1097-0223","type":"electronic"}],"subject":[],"published":{"date-parts":[[1984,3]]}}}