{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,5]],"date-time":"2025-10-05T19:52:54Z","timestamp":1759693974519},"reference-count":11,"publisher":"Wiley","issue":"10","license":[{"start":{"date-parts":[[2005,9,28]],"date-time":"2005-09-28T00:00:00Z","timestamp":1127865600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Prenatal Diagnosis"],"published-print":{"date-parts":[[2005,10]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>We present a case of prenatal diagnosis of a <jats:italic>de novo<\/jats:italic> (7;19)(q11.2;q13.3) translocation associated with ultrasound features, including enlarged cisterna magna, normal vermis, thick <jats:italic>corpus callosum<\/jats:italic>, micrognathia, small and low\u2010set ears and right hyperechogenic kidney. Karyotyping was performed at 24 weeks of gestation. Termination of pregnancy was accepted at the parents' request. Postmortem examination confirmed the prenatal findings, but revealed bilateral Wilms tumors of the kidneys. Parental karyotype was normal. Copyright \u00a9 2005 John Wiley &amp; Sons, Ltd.<\/jats:p>","DOI":"10.1002\/pd.1129","type":"journal-article","created":{"date-parts":[[2005,9,28]],"date-time":"2005-09-28T15:46:43Z","timestamp":1127922403000},"page":"876-878","source":"Crossref","is-referenced-by-count":10,"title":["Prenatal diagnosis of <i>de novo<\/i> (7;19)(q11.2;q13.3) translocation associated with a thick <i>corpus callosum<\/i> and Wilms tumor of the kidneys"],"prefix":"10.1002","volume":"25","author":[{"given":"Ottavia","family":"Cavicchioni","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Denise Molina","family":"Gomes","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Brigitte","family":"Leroy","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fran\u00e7ois","family":"Vialard","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yvette","family":"Hillion","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jacqueline","family":"Selva","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yves","family":"Ville","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2005,9,28]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1053\/jpsu.2002.32880"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1016\/0165-4608(82)90073-5"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.1097\/00008480-200202000-00002"},{"key":"e_1_2_1_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0268-960X(97)90006-0"},{"key":"e_1_2_1_6_1","doi-asserted-by":"publisher","DOI":"10.2214\/ajr.161.5.8273605"},{"issue":"7","key":"e_1_2_1_7_1","first-page":"1387","article-title":"Linkage of familial Wilms tumor predisposition to chromosome 19 and two locus model for the etiology of familial tumors","volume":"58","author":"McDonald JM","year":"1998","journal-title":"Cancer Res"},{"key":"e_1_2_1_8_1","doi-asserted-by":"publisher","DOI":"10.1016\/0006-3223(86)90048-X"},{"key":"e_1_2_1_9_1","doi-asserted-by":"publisher","DOI":"10.1097\/00019605-200404000-00006"},{"key":"e_1_2_1_10_1","first-page":"1918","article-title":"Prenatal MR diagnosis of a thick corpus callosum","volume":"17","author":"Rypens F","year":"1996","journal-title":"Am J Neuroradiol"},{"key":"e_1_2_1_11_1","doi-asserted-by":"publisher","DOI":"10.1016\/0165-4608(91)90148-N"},{"key":"e_1_2_1_12_1","first-page":"425","article-title":"Clinical applications of cytogenetic abnormalities in acute nonlymphocytic leukemia","volume":"3","author":"Trujillo JM","year":"1981","journal-title":"Am J Pediatr Hematol Oncol"}],"container-title":["Prenatal Diagnosis"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fpd.1129","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/obgyn.onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/pd.1129","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,11,17]],"date-time":"2023-11-17T02:54:31Z","timestamp":1700189671000},"score":1,"resource":{"primary":{"URL":"https:\/\/obgyn.onlinelibrary.wiley.com\/doi\/10.1002\/pd.1129"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2005,9,28]]},"references-count":11,"journal-issue":{"issue":"10","published-print":{"date-parts":[[2005,10]]}},"alternative-id":["10.1002\/pd.1129"],"URL":"https:\/\/doi.org\/10.1002\/pd.1129","archive":["Portico"],"relation":{},"ISSN":["0197-3851","1097-0223"],"issn-type":[{"value":"0197-3851","type":"print"},{"value":"1097-0223","type":"electronic"}],"subject":[],"published":{"date-parts":[[2005,9,28]]}}}