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 - Paulina

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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

scientific article published on 23 June 2020

Author/s

author: Kazuki Yamazawa, Tsutomu Ogata, Masayo Kagami, Keiko Matsubara, Kazuhiko Nakabayashi, Takanobu Inoue, Akie Nakamura, Kenichiro Hata

Work details

Publication date

June 23, 2020

Language

English

Copyright status

copyrighted