Array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus associated with split hand–foot malformation. Role of EPS15L1 in pathogenesis
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Format: | Article |
Language: | English |
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Elsevier
2015-08-01
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Series: | Taiwanese Journal of Obstetrics & Gynecology |
Online Access: | http://www.sciencedirect.com/science/article/pii/S1028455915001382 |
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author | Ya-Lien Hsueh Yi-Ning Su Hsin-Yu Lin Chien-Nan Lee Jin-Chung Shih |
author_facet | Ya-Lien Hsueh Yi-Ning Su Hsin-Yu Lin Chien-Nan Lee Jin-Chung Shih |
author_sort | Ya-Lien Hsueh |
collection | DOAJ |
first_indexed | 2024-04-13T10:03:36Z |
format | Article |
id | doaj.art-eab07d2d668848838ec763e111160ea7 |
institution | Directory Open Access Journal |
issn | 1028-4559 |
language | English |
last_indexed | 2024-04-13T10:03:36Z |
publishDate | 2015-08-01 |
publisher | Elsevier |
record_format | Article |
series | Taiwanese Journal of Obstetrics & Gynecology |
spelling | doaj.art-eab07d2d668848838ec763e111160ea72022-12-22T02:51:10ZengElsevierTaiwanese Journal of Obstetrics & Gynecology1028-45592015-08-0154445545810.1016/j.tjog.2014.12.009Array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus associated with split hand–foot malformation. Role of EPS15L1 in pathogenesisYa-Lien Hsueh0Yi-Ning Su1Hsin-Yu Lin2Chien-Nan Lee3Jin-Chung Shih4Department of Obstetrics and Gynecology, Cardinal Tien Hospital Yunghe Branch, New Taipei City, TaiwanDepartment of Obstetrics and Gynecology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, TaiwanDepartment of Obstetrics and Gynecology, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, TaiwanDepartment of Obstetrics and Gynecology, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, TaiwanDepartment of Obstetrics and Gynecology, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwanhttp://www.sciencedirect.com/science/article/pii/S1028455915001382 |
spellingShingle | Ya-Lien Hsueh Yi-Ning Su Hsin-Yu Lin Chien-Nan Lee Jin-Chung Shih Array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus associated with split hand–foot malformation. Role of EPS15L1 in pathogenesis Taiwanese Journal of Obstetrics & Gynecology |
title | Array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus associated with split hand–foot malformation. Role of EPS15L1 in pathogenesis |
title_full | Array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus associated with split hand–foot malformation. Role of EPS15L1 in pathogenesis |
title_fullStr | Array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus associated with split hand–foot malformation. Role of EPS15L1 in pathogenesis |
title_full_unstemmed | Array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus associated with split hand–foot malformation. Role of EPS15L1 in pathogenesis |
title_short | Array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus associated with split hand–foot malformation. Role of EPS15L1 in pathogenesis |
title_sort | array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22 1 7q11 23 7q21 3 q22 1 19p13 3 p12 and 19q13 11 q13 43 in a fetus associated with split hand foot malformation role of eps15l1 in pathogenesis |
url | http://www.sciencedirect.com/science/article/pii/S1028455915001382 |
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