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Genome-wide methylation analysis in Silver-Russell syndrome, Temple syndrome, and Prader-Willi syndrome.
Hara-Isono, Kaori; Matsubara, Keiko; Fuke, Tomoko; Yamazawa, Kazuki; Satou, Kazuhito; Murakami, Nobuyuki; Saitoh, Shinji; Nakabayashi, Kazuhiko; Hata, Kenichiro; Ogata, Tsutomu; Fukami, Maki; Kagami, Masayo.
Afiliação
  • Hara-Isono K; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan.
  • Matsubara K; Department of Pediatrics, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.
  • Fuke T; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan.
  • Yamazawa K; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan.
  • Satou K; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan.
  • Murakami N; Medical Genetics Center, National Hospital Organization Tokyo Medical Center, 2-5-1 Higashigaoka, Meguro-ku, Tokyo, 152-8902, Japan.
  • Saitoh S; Department of Genome Medicine, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan.
  • Nakabayashi K; Department of Pediatrics, Dokkyo Medical University Saitama Medical Center, 2-1-50 Minami Koshigaya, Koshigaya, 343-8555, Japan.
  • Hata K; Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya, 467-8601, Japan.
  • Ogata T; Department of Maternal Fetal Biology, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan.
  • Fukami M; Department of Maternal Fetal Biology, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan.
  • Kagami M; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan.
Clin Epigenetics ; 12(1): 159, 2020 10 22.
Article em En | MEDLINE | ID: mdl-33092629
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi / Polegar / Hallux / Síndrome de Silver-Russell / Deficiência Intelectual / Unhas Malformadas Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi / Polegar / Hallux / Síndrome de Silver-Russell / Deficiência Intelectual / Unhas Malformadas Idioma: En Ano de publicação: 2020 Tipo de documento: Article