{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,22]],"date-time":"2026-09-22T12:57:10Z","timestamp":1790081830814,"version":"4.0.1"},"reference-count":15,"publisher":"SAGE Publications","issue":"2","license":[{"start":{"date-parts":[[2016,3,1]],"date-time":"2016-03-01T00:00:00Z","timestamp":1456790400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["The Cleft Palate Craniofacial Journal"],"published-print":{"date-parts":[[2016,3]]},"abstract":"<jats:p>The oculoauriculovertebral spectrum or Goldenhar syndrome is characterized by varying degrees of prevalently unilateral underdevelopment of the craniofacial structures (orbit, ear, and mandible) in association with vertebral, cardiac, renal, and central nervous system defects. We report on a term neonate with a partial monosomy 7q21.11 with marked hemifacial microsomia, facial clefting, and spinal anomaly. The estimated size of the monosomic region of 7q21.11 was approximately 55 kilobases. This is the first report of a patient with partial monosomy 7q21.11 associated with oculoauriculovertebral spectrum.<\/jats:p>","DOI":"10.1597\/14-308","type":"journal-article","created":{"date-parts":[[2015,6,11]],"date-time":"2015-06-11T11:17:00Z","timestamp":1434021420000},"page":"249-252","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":6,"title":["7q21.11 Microdeletion in a Neonate with Goldenhar Syndrome: Case Report and a Literature Review"],"prefix":"10.1177","volume":"53","author":[{"given":"Surasak","family":"Puvabanditsin","sequence":"first","affiliation":[{"name":"Department of Pediatrics;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Melissa","family":"February","sequence":"additional","affiliation":[{"name":"Department of Pediatrics;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lissa","family":"Francois","sequence":"additional","affiliation":[{"name":"Department of Obstetrics and Gynecology, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Eugene","family":"Garrow","sequence":"additional","affiliation":[{"name":"Department of Surgery, State University of New York Downstate Medical Center, Brooklyn, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Chantal","family":"Bruno","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rajeev","family":"Mehta","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey."}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2018,1,3]]},"reference":[{"key":"bibr1-14-308","doi-asserted-by":"crossref","first-page":"3071","DOI":"10.1242\/dev.128.16.3071","volume":"128","author":"Brown C.B.","year":"2001","journal-title":"Development."},{"key":"bibr2-14-308","first-page":"276","volume":"26","author":"Cohen M.M.","year":"1989","journal-title":"Cleft Palate J."},{"key":"bibr3-14-308","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.30106"},{"key":"bibr4-14-308","unstructured":"GeneCards. 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