{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,2,21]],"date-time":"2025-02-21T08:28:13Z","timestamp":1740126493438,"version":"3.37.3"},"reference-count":15,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2018,3,8]],"date-time":"2018-03-08T00:00:00Z","timestamp":1520467200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"Medical Technology Breeding Project for PLA's Youth","award":["14QNP004"],"award-info":[{"award-number":["14QNP004"]}]},{"name":"Natural Science Foundation of Liaoning","award":["2015020423"],"award-info":[{"award-number":["2015020423"]}]},{"name":"Training Project of public welfare research of Liaoning","award":["2015001013"],"award-info":[{"award-number":["2015001013"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J of Obstet and Gynaecol"],"published-print":{"date-parts":[[2018,6]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Turner syndrome, characterized by the presence of a monosomy X cell line, is a common chromosomal disorder. Patients with Turner syndrome are usually phenotypically female, and male cases are rarely reported. Here, we report a fetus with a mosaic karyotype: mos 45,X\/46,X,del(Y)(q11.21). The fetus was initially misdiagnosed as female with Turner syndrome by both noninvasive prenatal testing and cytogenetic analysis of amniotic fluid and was subsequently found to have male anatomy by antenatal ultrasonography at 24 weeks gestational age. Through single nucleotide polymorphism\u2010array and fluorescence in situ hybridization testing, we found that there was a truncated Y chromosome with sex\u2010determining region Y (<jats:italic>SRY<\/jats:italic>) present in some cells of the fetus, which caused the male features in the fetus.<\/jats:p>","DOI":"10.1111\/jog.13617","type":"journal-article","created":{"date-parts":[[2018,3,8]],"date-time":"2018-03-08T11:22:39Z","timestamp":1520508159000},"page":"1158-1162","source":"Crossref","is-referenced-by-count":3,"title":["Mosaic male fetus of Turner syndrome with partial chromosome Y: A case report"],"prefix":"10.1111","volume":"44","author":[{"given":"Dan","family":"Xue","sequence":"first","affiliation":[{"name":"Department of Cardiovascular Ultrasound The First Hospital of China Medical University  Shenyang China"},{"name":"Department of Ultrasound No.202 Hospital of PLA  Shenyang China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dong\u2010Hua","family":"Cao","sequence":"additional","affiliation":[{"name":"Genetic Disease Laboratory Dalian Maternal and Child Health Care Hospital  Dalian China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kai","family":"Mu","sequence":"additional","affiliation":[{"name":"Genetic Disease Laboratory Zibo Maternal and Child Health Hospital  Zibo China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yuan","family":"Lv","sequence":"additional","affiliation":[{"name":"Gynaecology and Obstetrics Shengjing Hospital of China Medical University  Shenyang China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9801-3664","authenticated-orcid":false,"given":"Jun","family":"Yang","sequence":"additional","affiliation":[{"name":"Department of Cardiovascular Ultrasound The First Hospital of China Medical University  Shenyang China"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2018,3,8]]},"reference":[{"key":"e_1_2_6_2_1","doi-asserted-by":"publisher","DOI":"10.1210\/jc.2006-0558"},{"key":"e_1_2_6_3_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1977.tb00908.x"},{"key":"e_1_2_6_4_1","doi-asserted-by":"publisher","DOI":"10.1038\/346240a0"},{"key":"e_1_2_6_5_1","doi-asserted-by":"publisher","DOI":"10.1136\/adc.65.8.891"},{"key":"e_1_2_6_6_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.30815"},{"key":"e_1_2_6_7_1","doi-asserted-by":"publisher","DOI":"10.1159\/000076532"},{"key":"e_1_2_6_8_1","doi-asserted-by":"publisher","DOI":"10.14310\/horm.2002.1272"},{"key":"e_1_2_6_9_1","doi-asserted-by":"publisher","DOI":"10.1210\/jc.2011-0232"},{"key":"e_1_2_6_10_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0015-0282(01)02877-1"},{"key":"e_1_2_6_11_1","doi-asserted-by":"publisher","DOI":"10.1007\/s00431-011-1600-9"},{"key":"e_1_2_6_12_1","doi-asserted-by":"publisher","DOI":"10.1159\/000281468"},{"key":"e_1_2_6_13_1","doi-asserted-by":"publisher","DOI":"10.1210\/jc.2012-1388"},{"key":"e_1_2_6_14_1","doi-asserted-by":"publisher","DOI":"10.1542\/peds.104.2.304"},{"key":"e_1_2_6_15_1","doi-asserted-by":"publisher","DOI":"10.1093\/ajcp\/108.2.197"},{"key":"e_1_2_6_16_1","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0054977"}],"container-title":["Journal of Obstetrics and Gynaecology Research"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fjog.13617","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/obgyn.onlinelibrary.wiley.com\/doi\/pdf\/10.1111\/jog.13617","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,9,10]],"date-time":"2023-09-10T00:56:46Z","timestamp":1694307406000},"score":1,"resource":{"primary":{"URL":"https:\/\/obgyn.onlinelibrary.wiley.com\/doi\/10.1111\/jog.13617"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,3,8]]},"references-count":15,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2018,6]]}},"alternative-id":["10.1111\/jog.13617"],"URL":"https:\/\/doi.org\/10.1111\/jog.13617","archive":["Portico"],"relation":{},"ISSN":["1341-8076","1447-0756"],"issn-type":[{"type":"print","value":"1341-8076"},{"type":"electronic","value":"1447-0756"}],"subject":[],"published":{"date-parts":[[2018,3,8]]}}}