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PDFEpigenetics
Short report
Loss of imprinting of the human-specific imprinted gene ZNF597 causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndrome
- Correspondence to Dr Kazuki Yamazawa, Medical Genetics Center, National Hospital Organisation Tokyo Medical Center, Tokyo 152-8902, Japan; kyamazawa{at}keio.jp
Citation
Loss of imprinting of the human-specific imprinted gene ZNF597 causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndrome
Publication history
- Received March 18, 2020
- Revised May 12, 2020
- Accepted May 13, 2020
- First published June 23, 2020.
Online issue publication
May 21, 2021
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© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article 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, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.