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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.
Yamazawa K, Inoue T, Sakemi Y, Nakashima T, Yamashita H, Khono K, Fujita H, Enomoto K, Nakabayashi K, Hata K, Nakashima M, Matsunaga T, Nakamura A, Matsubara K, Ogata T, Kagami M. Yamazawa K, et al. Among authors: khono k. J Med Genet. 2021 Jun;58(6):427-432. doi: 10.1136/jmedgenet-2020-107019. Epub 2020 Jun 23. J Med Genet. 2021. PMID: 32576657 Free PMC article.