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Articles Published Processes
3/12/2024 6:10:26 AM | Browse: 182 | Download: 799
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Received |
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2023-12-13 19:32 |
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Peer-Review Started |
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2023-12-13 19:32 |
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First Decision by Editorial Office Director |
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2023-12-21 21:58 |
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Return for Revision |
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2023-12-21 21:58 |
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Revised |
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2024-01-22 20:06 |
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Publication Fee Transferred |
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Second Decision by Editor |
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2024-02-25 02:38 |
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Second Decision by Editor-in-Chief |
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Final Decision by Editorial Office Director |
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2024-02-25 07:45 |
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Articles in Press |
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2024-02-25 07:45 |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2024-03-04 08:10 |
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Publish the Manuscript Online |
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2024-03-12 06:10 |
| ISSN |
2307-8960 (online) |
| Open Access |
This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/ |
| Copyright |
© The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved. |
| Article Reprints |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
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| Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
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| Publisher |
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA |
| Website |
http://www.wjgnet.com |
| Category |
Genetics & Heredity |
| Manuscript Type |
Case Report |
| Article Title |
Detection of 4p16.3 deletion and 11p15.5p15.4 gain in a boy by comparative genomic hybridization array: A case report
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| Manuscript Source |
Unsolicited Manuscript |
| All Author List |
Işın Kaya |
| ORCID |
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| Funding Agency and Grant Number |
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| Corresponding Author |
Işın Kaya, MD, Doctor, Doctor, Medical Genetics, Bakırçay University Çiğli Education ve Training Hospital, Yeni Mahalle, 8780/1. Street. No. 18 Çiğli, İzmir 35620, Türkiye. isintkaya@yahoo.com |
| Key Words |
Wolf-Hirschhorn syndrome; Silver-Russell syndrome; Recurrent rearrangements; Case report |
| Core Tip |
Chromosome analysis of a young child with developmental delay, cleft palate, hearing loss, and mental retardation indicated 46, XY. Further genetic analysis with comparative genomic hybridization array revealed a deletion in the short arm of chromosome 4 and a gain in the short arm of chromosome 11. The patient’s phenotypic findings were associated with the genes affected by the genomic loss and gain. |
| Publish Date |
2024-03-12 06:10 |
| Citation |
Kaya I. Detection of 4p16.3 deletion and 11p15.5p15.4 gain in a boy by comparative genomic hybridization array: A case report. World J Clin Cases 2024; 12(8): 1517-1522 |
| URL |
https://www.wjgnet.com/2307-8960/full/v12/i8/1517.htm |
| DOI |
https://dx.doi.org/10.12998/wjcc.v12.i8.1517 |
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