{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,2,21]],"date-time":"2025-02-21T18:55:41Z","timestamp":1740164141104,"version":"3.37.3"},"reference-count":7,"publisher":"Wiley","license":[{"start":{"date-parts":[[2016,1,1]],"date-time":"2016-01-01T00:00:00Z","timestamp":1451606400000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Case Reports in Genetics"],"published-print":{"date-parts":[[2016]]},"abstract":"<jats:p>Proximal duplications of chromosome 1q are rare chromosomal abnormalities. Most patients with this condition present with neurological, urogenital, and congenital heart disease and short life expectancy. Mosaicism for trisomy 1q10q23.3 has only been reported once in the literature. Here we discuss a second case: a girl with a postnatal diagnosis of a<jats:italic>de novo<\/jats:italic>pure mosaic trisomy 1q1023.3 who has no urogenital or cardiac anomalies.<\/jats:p>","DOI":"10.1155\/2016\/2861653","type":"journal-article","created":{"date-parts":[[2016,1,31]],"date-time":"2016-01-31T16:05:01Z","timestamp":1454256301000},"page":"1-5","source":"Crossref","is-referenced-by-count":1,"title":["<i>De Novo<\/i>Trisomy 1q10q23.3 Mosaicism Causes Microcephaly, Severe Developmental Delay, and Facial Dysmorphic Features but No Cardiac Anomalies"],"prefix":"10.1155","volume":"2016","author":[{"given":"Shirley","family":"Lo-A-Njoe","sequence":"first","affiliation":[{"name":"Department of Pediatrics, Horacio Oduber Hospital, Oranjestad, Aruba"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lars T.","family":"van der Veken","sequence":"additional","affiliation":[{"name":"Department of Genetics, Wilhelmina Children\u2019s Hospital, UMC Utrecht, 3584 EA Utrecht, Netherlands"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2219-856X","authenticated-orcid":true,"given":"Clementien","family":"Vermont","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Horacio Oduber Hospital, Oranjestad, Aruba"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Louise","family":"Rafael-Croes","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Horacio Oduber Hospital, Oranjestad, Aruba"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2275-1361","authenticated-orcid":true,"given":"Vincent","family":"Keizer","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Horacio Oduber Hospital, Oranjestad, Aruba"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ron","family":"Hochstenbach","sequence":"additional","affiliation":[{"name":"Department of Genetics, Wilhelmina Children\u2019s Hospital, UMC Utrecht, 3584 EA Utrecht, Netherlands"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nine","family":"Knoers","sequence":"additional","affiliation":[{"name":"Department of Genetics, Wilhelmina Children\u2019s Hospital, UMC Utrecht, 3584 EA Utrecht, Netherlands"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mieke M.","family":"van Haelst","sequence":"additional","affiliation":[{"name":"Department of Genetics, Wilhelmina Children\u2019s Hospital, UMC Utrecht, 3584 EA Utrecht, Netherlands"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","reference":[{"key":"1","doi-asserted-by":"publisher","DOI":"10.1002\/pd.2061"},{"key":"2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1987.tb03322.x"},{"key":"3","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.30588"},{"key":"4","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.32959"},{"key":"5","doi-asserted-by":"publisher","DOI":"10.1002\/bdra.23213"},{"key":"6","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1285"},{"year":"2013","series-title":"edited by L. 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