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Articles Published Processes
11/6/2020 9:07:37 AM | Browse: 413 | Download: 1052
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Received |
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2020-07-13 16:26 |
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Peer-Review Started |
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2020-07-13 16:26 |
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To Make the First Decision |
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Return for Revision |
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2020-08-08 02:16 |
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Revised |
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2020-09-08 15:37 |
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Second Decision |
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2020-09-17 12:21 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2020-09-17 17:58 |
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Articles in Press |
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2020-09-17 17:58 |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2020-10-26 04:11 |
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Publish the Manuscript Online |
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2020-11-06 09:07 |
| 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: http://creativecommons.org/Licenses/by-nc/4.0/ |
| Copyright |
© The Author(s) 2020. 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 |
Medicine, Research & Experimental |
| Manuscript Type |
Case Report |
| Article Title |
Submicroscopic 11p13 deletion including the elongator acetyltransferase complex subunit 4 gene in a girl with language failure, intellectual disability and congenital malformations: A case report
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| Manuscript Source |
Unsolicited Manuscript |
| All Author List |
Jaime Toral-Lopez, Luz María González Huerta, Olga Messina-Baas and Sergio A Cuevas-Covarrubias |
| ORCID |
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| Funding Agency and Grant Number |
| Funding Agency |
Grant Number |
| PAEP, 2018 and PAPIIT IN219419, DGAPA, Universidad Nacional Autónoma de México |
IN219419 |
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| Corresponding Author |
Sergio A Cuevas-Covarrubias, PhD, Doctor, Doctor, Professor, Genetica, Hospital General de México, Dr Balmis 148, Cuauhtémoc 06726, Mexico. sercuevas@yahoo.com |
| Key Words |
Submicroscopic 11p13 deletion; Elongator acetyltransferase complex subunit 4 gene; Language failure; Intellectual disability; Congenital malformations; Case report |
| Core Tip |
We report a case diagnosed with submicroscopic 11p13 deletion. The main clinical characteristics and elongator acetyltransferase complex subunit 4 gene deletion, and treatments were assessed and a review of the related literature was performed. Very important, this is the second case of deletion of the elongator acetyltransferase complex subunit 4 gene without aniridia. |
| Publish Date |
2020-11-06 09:07 |
| Citation |
Toral-Lopez J, González Huerta LM, Messina-Baas O, Cuevas-Covarrubias SA. Submicroscopic 11p13 deletion including the elongator acetyltransferase complex subunit 4 gene in a girl with language failure, intellectual disability and congenital malformations: A case report. World J Clin Cases 2020; 8(21): 5296-5303 |
| URL |
https://www.wjgnet.com/2307-8960/full/v8/i21/5296.htm |
| DOI |
https://dx.doi.org/10.12998/wjcc.v8.i21.5296 |
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