Loss of imprinting of the human-specific imprinted gene <i>ZNF597</i> causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndrome.

Yamazawa, Kazuki; Inoue, Takanobu; Sakemi, Yoshihiro; Nakashima, Toshinori; Yamashita, Hironori; Khono, Kaduki; Fujita, Hideki; Enomoto, Keisuke; Nakabayashi, Kazuhiko; Hata, Kenichiro; Nakashima, Moeko; Matsunaga, Tatsuo; Nakamura, Akie; Matsubara, Keiko; Ogata, Tsutomu; Kagami, Masayo

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, Kazuki; Inoue, Takanobu; Sakemi, Yoshihiro; Nakashima, Toshinori; Yamashita, Hironori; Khono, Kaduki; Fujita, Hideki; Enomoto, Keisuke; Nakabayashi, Kazuhiko; Hata, Kenichiro; Nakashima, Moeko; Matsunaga, Tatsuo; Nakamura, Akie; Matsubara, Keiko; Ogata, Tsutomu; Kagami, Masayo.

Afiliação

Yamazawa K; Medical Genetics Center, National Hospital Organization Tokyo Medical Center, Tokyo, Japan kyamazawa@keio.jp.
Inoue T; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.
Sakemi Y; Department of Pediatrics, University of Tokyo, Tokyo, Japan.
Nakashima T; Department of Pediatrics, National Hospital Organization Kokura Medical Center, Kitakyushu, Japan.
Yamashita H; Department of Pediatrics, National Hospital Organization Kokura Medical Center, Kitakyushu, Japan.
Khono K; Department of Pediatrics, National Hospital Organization Kokura Medical Center, Kitakyushu, Japan.
Fujita H; Navitas Clinic Kawasaki, Kawasaki, Japan.
Enomoto K; Meguro Avenue Kid's Clinic, Tokyo, Japan.
Nakabayashi K; Enomoto Children's Clinic, Moriya, Japan.
Hata K; Department of Maternal-Fetal Biology, National Research Institute for Child Health and Development, Tokyo, Japan.
Nakashima M; Department of Maternal-Fetal Biology, National Research Institute for Child Health and Development, Tokyo, Japan.
Matsunaga T; Medical Genetics Center, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
Nakamura A; Medical Genetics Center, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
Matsubara K; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.
Ogata T; Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Kagami M; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.

J Med Genet ; 58(6): 427-432, 2021 06.

Article em En | MEDLINE | ID: mdl-32576657

Assuntos

Anormalidades Múltiplas/genética; Retardo do Crescimento Fetal/genética; Impressão Genômica; Fatores de Transcrição/genética; Criança; Metilação de DNA; Humanos; Masculino; Síndrome de Silver-Russell/genética

Palavras-chave

DNA methylation; genetics, medical

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Anormalidades Múltiplas / Impressão Genômica / Retardo do Crescimento Fetal Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Child / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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