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.

MLA

Kazuki Yamazawa, et al. “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.” Journal of Medical Genetics, vol. 58, no. 6, June 2021, pp. 427–32. EBSCOhost, https://doi.org/10.1136/jmedgenet-2020-107019.

APA

Kazuki Yamazawa, Takanobu Inoue, Yoshihiro Sakemi, Toshinori Nakashima, Hironori Yamashita, Kaduki Khono, Hideki Fujita, Keisuke Enomoto, Kazuhiko Nakabayashi, Kenichiro Hata, Moeko Nakashima, Tatsuo Matsunaga, Akie Nakamura, Keiko Matsubara, Tsutomu Ogata, & Masayo Kagami. (2021). 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. Journal of Medical Genetics, 58(6), 427–432. https://doi.org/10.1136/jmedgenet-2020-107019

Chicago

Kazuki Yamazawa, Takanobu Inoue, Yoshihiro Sakemi, Toshinori Nakashima, Hironori Yamashita, Kaduki Khono, Hideki Fujita, et al. 2021. “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.” Journal of Medical Genetics 58 (6): 427–32. doi:10.1136/jmedgenet-2020-107019.