BPG is committed to discovery and dissemination of knowledge
Featured Articles
3/1/2021 5:51:10 AM | Browse: 256 | Download: 1059
Publication Name World Journal of Clinical Cases
Manuscript ID 60876
Country/Territory China
Received
2020-11-23 11:25
Peer-Review Started
2020-11-23 11:25
To Make the First Decision
Return for Revision
2020-12-08 06:55
Revised
2020-12-10 00:20
Second Decision
2020-12-24 08:29
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief
2020-12-25 05:41
Articles in Press
2020-12-25 05:41
Publication Fee Transferred
Edit the Manuscript by Language Editor
2021-01-14 01:29
Typeset the Manuscript
2021-02-18 02:15
Publish the Manuscript Online
2021-03-01 03:51
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
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 Pediatrics
Manuscript Type Retrospective Study
Article Title Study on pathogenic genes of dwarfism disease by next-generation sequencing
Manuscript Source Unsolicited Manuscript
All Author List Lv-Lv Yang and Shi-Shan Liang
Funding Agency and Grant Number
Funding Agency Grant Number
Quanzhou Science and Technology Bureau 2018Z072
Corresponding Author Lv-Lv Yang, MD, Doctor, Department of Pediatrics, Quanzhou First Hospital, No. 248-252 East Street, Licheng District, Quanzhou 362000, Fujian Province, China. lvlv8000@126.com
Key Words Dwarfism; Next-generation sequencing; Pathogenicity variability; Growth hormone; Therapy; Mechanism
Core Tip Genetic variation may relate to the incidence of dwarfism. After Solexa sequencing, the OBSL1, SLC26A2, PTPN11, COL27AI, HDAC6, CUL7, FGFR3, DYNC2H1, GH1, and ATP7B genes may be related to dwarfism and clarify the molecular cause.
Publish Date 2021-03-01 03:51
Citation Yang LL, Liang SS. Study on pathogenic genes of dwarfism disease by next-generation sequencing. World J Clin Cases 2021; 9(7): 1600-1609
URL https://www.wjgnet.com/2307-8960/full/v9/i7/1600.htm
DOI https://dx.doi.org/10.12998/wjcc.v9.i7.1600
Full Article (PDF) WJCC-9-1600.pdf
Full Article (Word) WJCC-9-1600.docx
Manuscript File 60876-Review-Filipodia_CL.docx
Answering Reviewers 60876-Answering reviewers.pdf
Audio Core Tip 60876-Audio core tip.mp3
Biostatistics Review Certificate 60876-Biostatistics statement.pdf
Conflict-of-Interest Disclosure Form 60876-Conflict-of-interest statement.pdf
Copyright License Agreement 60876-Copyright license agreement.pdf
Approved Grant Application Form(s) or Funding Agency Copy of any Approval Document(s) 60876-Grant application form(s).pdf
Signed Informed Consent Form(s) or Document(s) 60876-Informed consent statement.pdf
Institutional Review Board Approval Form or Document 60876-Institutional review board statement.pdf
Non-Native Speakers of English Editing Certificate 60876-Language certificate.pdf
Peer-review Report 60876-Peer-review(s).pdf
Scientific Misconduct Check 60876-Bing-Fan JR-1.png
Scientific Misconduct Check 60876-Scientific misconduct check.pdf
Scientific Editor Work List 60876-Scientific editor work list.pdf