Publication Name	World Journal of Orthopedics
Manuscript ID	24213
Country	United Kingdom

Received	2016-01-13 08:51
Peer-Review Started	2016-01-15 09:04
To Make the First Decision	2016-03-25 14:40
Return for Revision	2016-03-25 16:21
Revised	2016-08-15 04:50
Second Decision	2016-09-12 09:58
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2016-09-22 14:23
Articles in Press	2016-09-22 14:23
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2016-11-25 13:47
Publish the Manuscript Online	2016-12-07 15:36

ISSN	2218-5836 (online)
Open Access	This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (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) 2016. Published by Baishideng Publishing Group Inc. All rights reserved.
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Category	Orthopedics
Manuscript Type	Case Report
Article Title	Recurrent missense mutation of GDF5 (p.R438L) causes proximal symphalangism in a British family
Manuscript Source	Invited Manuscript
All Author List	Andreas Leonidou, Melita Irving, Simon Holden and Marcos Katchburian
Funding Agency and Grant Number
Corresponding Author	Andreas Leonidou, PgDip, MSc, FRCS(Orth), Specialist Registrar, Department of Trauma and Orthopaedic Surgery, Maidstone and Tunbridge Wells NHS Trust, Tonbridge Road, Pembury, Tunbridge Wells TN2 4QJ, United Kingdom. leonidou@doctors.org.uk
Key Words	Proximal symphalangism; GDF5
Core Tip	This report highlights the importance of thorough history taking, including a three generation family history, and detailed clinical examination of children with fixed planovalgus feet and other family members to detect rare skeletal dysplasia conditions causing pain and deformity, and provides details of the spectrum of problems associated with SYM1B.
Publish Date	2016-12-07 15:36
Citation	Leonidou A, Irving M, Holden S, Katchburian M. Recurrent missense mutation of GDF5 (p.R438L) causes proximal sympha¬langism in a British family. World J Orthop 2016; 7(12): 839-842
URL	http://www.wjgnet.com/2218-5836/full/v7/i12/839.htm
DOI	http://dx.doi.org/10.5312/wjo.v7.i12.839

Full Article (PDF)	WJO-7-839.pdf
Full Article (Word)	WJO-7-839.doc
Manuscript File	24213-Reivew.docx
Answering Reviewers	24213-Answering reviewers.pdf
Audio Core Tip	24213-Audio core tip.mp4
Conflict-of-Interest Disclosure Form	24213-Conflict-of-interest statement.pdf
Copyright License Agreement	24213-Copyright assignment.pdf
Peer-review Report	24213-Peer-review(s).pdf
Scientific Misconduct Check	24213-Scientific misconduct check.pdf
Scientific Editor Work List	24213-Scientific editor work list.pdf