Publication Name	World Journal of Clinical Cases
Manuscript ID	60876
Country	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 Executive 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/
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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
ORCID	Author(s) ORCID Number Lv-Lv Yang http://orcid.org/0000-0003-0237-9205 Shi-Shan Liang http://orcid.org/0000-0002-5164-6106
Funding Agency and Grant Number	Funding Agency Grant Number Quanzhou Science and Technology Bureau 2018Z072
Corresponding Author	Lv-Lv Yang, MD, Doctor, 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
CrossCheck Report	60876-CrossCheck report.pdf