Uniparental disomy as a mechanism for X-linked chondrodysplasia punctata

Woods, E., Yates, M., Kanani, F. et al. (1 more author) (2022) Uniparental disomy as a mechanism for X-linked chondrodysplasia punctata. Clinical Dysmorphology. ISSN 0962-8827

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Authors/Creators:
Copyright, Publisher and Additional Information: © 2022 Wolters Kluwer Health. This is an author-produced version of a paper subsequently published in Clinical Dysmorphology. This version is distributed under the terms of the Creative Commons Attribution-NonCommercial Licence (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. You may not use the material for commercial purposes.
Dates:
  • Published (online): 7 March 2022
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > Department of Human Metabolism (Sheffield)
The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > Department of Oncology (Sheffield)
Depositing User: Symplectic Sheffield
Date Deposited: 21 Apr 2022 11:18
Last Modified: 21 Apr 2022 13:17
Status: Published online
Publisher: Ovid Technologies (Wolters Kluwer Health)
Refereed: Yes
Identification Number: https://doi.org/10.1097/mcd.0000000000000419
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