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She showed no signs of hypotelorism, upslanting palpebral fissures, epicanthal folds, low-set ears, or flat and broad nasal bridge. Microarray testing using the Affymetrix CytoScan HD array revealed an approximately 58 kb deletion at 7q31.1 in the girl and her father, suggesting paternal origin. As the patient had no characteristic facial features, 7q deletions had not been considered. This case broadens the range of case presentations for microdeletions of chromosome 7.<\/jats:p>","DOI":"10.1515\/med-2018-0064","type":"journal-article","created":{"date-parts":[[2018,10,3]],"date-time":"2018-10-03T05:01:10Z","timestamp":1538542870000},"page":"433-435","source":"Crossref","is-referenced-by-count":3,"title":["Partial deletion of the long arm of chromosome 7: a case report"],"prefix":"10.1515","volume":"13","author":[{"given":"Chun","family":"Zhu","sequence":"first","affiliation":[{"name":"Department of Child Health Care , The Affiliated Obstetrics and Gynecology Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital , Nanjing , Jiangsu 210004 , China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mei-Ling","family":"Tong","sequence":"additional","affiliation":[{"name":"Department of Child Health Care , The Affiliated Obstetrics and Gynecology Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital , Nanjing , Jiangsu 210004 , China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xia","family":"Chi","sequence":"additional","affiliation":[{"name":"Department of Child Health Care , The Affiliated Obstetrics and Gynecology Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital , Nanjing , Jiangsu 210004 , China"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"374","published-online":{"date-parts":[[2018,9,29]]},"reference":[{"key":"2022042708343411452_j_med-2018-0064_ref_001_w2aab3b7d312b1b6b1ab2b2b1Aa","doi-asserted-by":"crossref","unstructured":"Weise A, Mrasek K, Klein E, Mulatinho M, Llerena JC Jr, Hardekopf D et al: Microdeletion and microduplication syndromes. 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