Publication Name	World Journal of Clinical Cases
Manuscript ID	84452
Country	China

Received	2023-03-14 15:54
Peer-Review Started	2023-03-14 15:56
To Make the First Decision
Return for Revision	2023-03-28 07:59
Revised	2023-04-06 04:05
Second Decision	2023-04-14 03:18
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2023-04-14 09:15
Articles in Press	2023-04-14 09:15
Publication Fee Transferred
Edit the Manuscript by Language Editor	2023-04-20 14:24
Typeset the Manuscript	2023-05-22 10:40
Publish the Manuscript Online	2023-06-02 11:04

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/
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Category	Pediatrics
Manuscript Type	Case Report
Article Title	Novel mutation c.2090_2091del in neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities of an 18.5-mo boy: A case report
Manuscript Source	Unsolicited Manuscript
All Author List	Yi Li, Zheng Zhou, Yan Xu and Zhi-Ru Wang
Funding Agency and Grant Number	Funding Agency Grant Number Joint Funds of the National Natural Science Foundation of China 82205190 Foundation for Distinguished Young Talents in Higher Education of Henan [2018]16
Corresponding Author	Zheng Zhou, Doctor, Chief Physician, Department of Pediatrics, The First Affiliated Hospital, Henan University of Chinese Medicine, No.19, Renmin Road, Jinshui District, Zhengzhou 450000, Henan Province, China. czj6799@126.com
Key Words	ZMYM2; NECRC; Frameshift mutation; Global developmental delay; Case report
Core Tip	Li Y, Zhou Z, Xu Y, Wang ZR. Novel mutation c.2090_2091del in NECRC of an 18.5-mo boy: A case report. World J Clin Cases 2023; In press
Publish Date	2023-06-02 11:04
Citation	Li Y, Zhou Z, Xu Y, Wang ZR. Novel mutation c.2090_2091del in neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities of an 18.5-mo boy: A case report. World J Clin Cases 2023; 11(16): 3891-3898
URL	https://www.wjgnet.com/2307-8960/full/v11/i16/3891.htm
DOI	https://dx.doi.org/10.12998/wjcc.v11.i16.3891

Full Article (PDF)	WJCC-11-3891.pdf
Full Article (Word)	WJCC-11-3891.docx
Manuscript File	84452_Auto_Edited-JLW-Language editing-Webster J-Clear.docx
Answering Reviewers	84452-Answering reviewers.pdf
Audio Core Tip	84452-Audio core tip.m4a
Conflict-of-Interest Disclosure Form	84452-Conflict-of-interest_statement.pdf
Copyright License Agreement	84452-Copyright license agreement.pdf
Approved Grant Application Form(s) or Funding Agency Copy of any Approval Document(s)	84452-Grant application form(s).pdf
Signed Consent for Treatment Form(s) or Document(s)	84452-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	84452-Language certificate.pdf
Peer-review Report	84452-Peer-review(s).pdf
Scientific Misconduct Check	84452-Bing-Liu XF-2.png
Scientific Editor Work List	84452-Scientific editor work list.pdf