BPG is committed to discovery and dissemination of knowledge
Articles Published Processes
6/17/2020 10:13:08 AM | Browse: 794 | Download: 733
 |
Received |
|
2020-03-14 19:43 |
|
Peer-Review Started |
|
2020-03-14 19:43 |
 |
To Make the First Decision |
|
|
|
Return for Revision |
|
2020-04-12 22:43 |
|
Revised |
|
2020-04-19 08:04 |
|
Second Decision |
|
2020-05-13 08:53 |
|
Accepted by Journal Editor-in-Chief |
|
|
|
Accepted by Company Editor-in-Chief |
|
2020-05-14 21:47 |
|
Articles in Press |
|
2020-05-14 21:47 |
|
Publication Fee Transferred |
|
|
|
Edit the Manuscript by Language Editor |
|
2020-05-21 23:15 |
|
Typeset the Manuscript |
|
2020-06-10 02:06 |
|
Publish the Manuscript Online |
|
2020-06-17 10:13 |
| ISSN |
2220-3184 (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 |
Genetics & Heredity |
| Manuscript Type |
Review |
| Article Title |
Clinical and molecular spectrum of Wiedemann-Steiner syndrome, an emerging member of the chromatinopathy family
|
| Manuscript Source |
Invited Manuscript |
| All Author List |
Paolo Fontana, Francesco Fioravanti Passaretti, Marianna Maioli, Giuseppina Cantalupo, Francesca Scarano and Fortunato Lonardo |
| ORCID |
|
| Funding Agency and Grant Number |
|
| Corresponding Author |
Fortunato Lonardo, MD, Chief Doctor, Medical Genetics Unit, San Pio Hospital, Via dell’Angelo, 1, Benevento 82100, BN, Italy. fortunato.lonardo@ao-rummo.it |
| Key Words |
Chromatin; Chromatin remodeling; Chromatinopathies; Wiedemann-Steiner syndrome; Hairy elbows; KMT2A |
| Core Tip |
Chromatinopathies are a highly heterogeneous group of syndromic conditions in which the underlying genetic anomaly consists of disruption of one of the components of the epigenetic machinery. Within this group, to which belong at more than 40 diseases, including Kabuki, Sotos, Kleefstra, Koolen-De-Vries/KANSL1 haploinsufficiency, Rubinstein-Taybi, KAT6B-related syndromes, Smith-Magenis, Rett, Townes-Brock, Bohring-Opitz, ATRX, CHARGE, Floating-Harbor syndromes, and an emerging member is represented by Wiedemann-Steiner syndrome, which has very interesting features. |
| Publish Date |
2020-06-17 10:13 |
| Citation |
Fontana P, Passaretti FF, Maioli M, Cantalupo G, Scarano F, Lonardo F. Clinical and molecular spectrum of Wiedemann-Steiner syndrome, an emerging member of the chromatinopathy family. World J Med Genet 2020; 9(1): 1-11 |
| URL |
https://www.wjgnet.com/2220-3184/full/v9/i1/1.htm |
| DOI |
https://dx.doi.org/10.5496/wjmg.v9.i1.1 |
© 2004-2024 Baishideng Publishing Group Inc. All rights reserved. 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
California Corporate Number: 3537345
