{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,2,21]],"date-time":"2025-02-21T18:55:26Z","timestamp":1740164126704,"version":"3.37.3"},"reference-count":11,"publisher":"Wiley","license":[{"start":{"date-parts":[[2012,1,1]],"date-time":"2012-01-01T00:00:00Z","timestamp":1325376000000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/3.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Case Reports in Genetics"],"published-print":{"date-parts":[[2012]]},"abstract":"<jats:p>Monosomy of chromosome 14 has been reported in only a few prenatal cases. Generally, this monosomy is associated with a mosaicism of ring chromosome 14. Ring chromosome 14 is a rare cytogenetic entity with clinical characteristics that include growth retardation, facial dysmorphia, hypotonia, seizures, and retinitis pigmentosa. Given that the majority of symptoms appear postnatally, few cases have been reported of prenatal diagnosis of mosaicism monosomy\/ring chromosome 14. We describe the prenatal diagnosis of a case of chromosomal mosaicism, a cell line with ring chromosome 14, r(14), and a second cell line with monosomy 14, in a fetus with aortic coarctation and chamber asymmetry. This is the first case of a prenatal diagnosis associating mosaicism with ring chromosome 14, monosomy 14, and fetal cardiopathy. We identified the exact breakpoint in ring chromosome 14 in IGH locus, which may provide further insight into the mode of ring formation as well as prenatal findings.<\/jats:p>","DOI":"10.1155\/2012\/794075","type":"journal-article","created":{"date-parts":[[2012,11,5]],"date-time":"2012-11-05T16:41:28Z","timestamp":1352133688000},"page":"1-4","source":"Crossref","is-referenced-by-count":1,"title":["Prenatal Diagnosis of a Fetus with Congenital Heart Defect and Ring Chromosome 14"],"prefix":"10.1155","volume":"2012","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-7315-9790","authenticated-orcid":true,"given":"Javier","family":"S\u00e1nchez","sequence":"first","affiliation":[{"name":"Unidad de Gesti\u00f3n Cl\u00ednica de Gen\u00e9tica, Reproducci\u00f3n y Medicina Fetal, Instituto de Biomedicina de Sevilla (IBIS), Hospital Universitario Virgen del Roc\u00edo (CSIC), Universidad de Sevilla, 41013 Seville, Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lutgardo","family":"Garc\u00eda-D\u00edaz","sequence":"additional","affiliation":[{"name":"Unidad de Gesti\u00f3n Cl\u00ednica de Gen\u00e9tica, Reproducci\u00f3n y Medicina Fetal, Instituto de Biomedicina de Sevilla (IBIS), Hospital Universitario Virgen del Roc\u00edo (CSIC), Universidad de Sevilla, 41013 Seville, Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"David","family":"Chinch\u00f3n","sequence":"additional","affiliation":[{"name":"Unidad de Gesti\u00f3n Cl\u00ednica de Anatom\u00eda Patol\u00f3gica, Hospital Universitario Virgen del Roc\u00edo, 41013 Seville, Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Guillermo","family":"Anti\u00f1olo","sequence":"additional","affiliation":[{"name":"Unidad de Gesti\u00f3n Cl\u00ednica de Gen\u00e9tica, Reproducci\u00f3n y Medicina Fetal, Instituto de Biomedicina de Sevilla (IBIS), Hospital Universitario Virgen del Roc\u00edo (CSIC), Universidad de Sevilla, 41013 Seville, Spain"},{"name":"Centro de Investigaci\u00f3n Biom\u00e9dica en Red de Enfermedades Raras (CIBERER), 46010 Valencia, Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","reference":[{"key":"2","first-page":"367","volume":"31","year":"1983","journal-title":"Journal de G\u00e9n\u00e9tique Humaine"},{"key":"9","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.32831"},{"key":"3","doi-asserted-by":"publisher","DOI":"10.1016\/S0015-0282(97)81874-2"},{"key":"5","doi-asserted-by":"publisher","DOI":"10.1097\/01.mcd.0000126137.29572.59"},{"key":"7","doi-asserted-by":"publisher","DOI":"10.1002\/pd.1911"},{"key":"11","doi-asserted-by":"publisher","DOI":"10.4238\/vol9-1gmr707"},{"key":"4","doi-asserted-by":"publisher","DOI":"10.1016\/S1383-5742(96)00052-X"},{"key":"1","doi-asserted-by":"publisher","DOI":"10.1038\/ejhg.2008.71"},{"key":"10","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.31438"},{"key":"12","doi-asserted-by":"publisher","DOI":"10.1097\/MCD.0b013e3283438200"},{"issue":"5","key":"6","doi-asserted-by":"crossref","first-page":"443","DOI":"10.1002\/(SICI)1096-8628(19981228)80:5<443::AID-AJMG2>3.0.CO;2-Y","volume":"80","year":"1998","journal-title":"American Journal of Medical Genetics"}],"container-title":["Case Reports in Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/downloads.hindawi.com\/journals\/crig\/2012\/794075.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/downloads.hindawi.com\/journals\/crig\/2012\/794075.xml","content-type":"application\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/downloads.hindawi.com\/journals\/crig\/2012\/794075.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2017,6,20]],"date-time":"2017-06-20T22:19:27Z","timestamp":1497997167000},"score":1,"resource":{"primary":{"URL":"http:\/\/www.hindawi.com\/journals\/crig\/2012\/794075\/"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012]]},"references-count":11,"alternative-id":["794075","794075"],"URL":"https:\/\/doi.org\/10.1155\/2012\/794075","relation":{},"ISSN":["2090-6544","2090-6552"],"issn-type":[{"type":"print","value":"2090-6544"},{"type":"electronic","value":"2090-6552"}],"subject":[],"published":{"date-parts":[[2012]]}}}