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3/12/2024 6:10:26 AM | Browse: 152 | Download: 655
Publication Name World Journal of Clinical Cases
Manuscript ID 90798
Country Türkiye
Received
2023-12-13 19:32
Peer-Review Started
2023-12-13 19:32
First Decision by Editorial Office Director
2023-12-21 21:58
Return for Revision
2023-12-21 21:58
Revised
2024-01-22 20:06
Publication Fee Transferred
Second Decision by Editor
2024-02-25 02:38
Second Decision by Editor-in-Chief
Final Decision by Editorial Office Director
2024-02-25 07:45
Articles in Press
2024-02-25 07:45
Edit the Manuscript by Language Editor
Typeset the Manuscript
2024-03-04 08:10
Publish the Manuscript Online
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
Permissions For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
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
Manuscript Source Unsolicited Manuscript
All Author List Işın Kaya
ORCID
Author(s) ORCID Number
Işın Kaya http://orcid.org/0000-0002-6293-8964
Funding Agency and Grant Number
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
Full Article (PDF) WJCC-12-1517-with-cover.pdf
CARE Checklist–2016 90798-CARE-Checklist–2016.pdf
Manuscript File 90798_Auto_Edited-YJP.docx
Answering Reviewers 90798-Answering reviewers.pdf
Audio Core Tip 90798-Audio core tip.m4a
Conflict-of-Interest Disclosure Form 90798-Conflict-of-interest statement.pdf
Copyright License Agreement 90798-Copyright license agreement.pdf
Signed Consent for Treatment Form(s) or Document(s) 90798-Informed consent statement.pdf
Peer-review Report 90798-Peer-review(s).pdf
Scientific Misconduct Check 90798-CrossCheck.png
Scientific Misconduct Check 90798-Bing-Wang JL-2.png
Scientific Editor Work List 90798-Scientific editor work list.pdf
CrossCheck Report 90798-CrossCheck report.pdf