Your browser doesn't support javascript.
loading
Genetic heterogeneity of patients with suspected Silver-Russell syndrome: genome-wide copy number analysis in 82 patients without imprinting defects.
Inoue, Takanobu; Nakamura, Akie; Fuke, Tomoko; Yamazawa, Kazuki; Sano, Shinichiro; Matsubara, Keiko; Mizuno, Seiji; Matsukura, Yoshika; Harashima, Chie; Hasegawa, Tatsuji; Nakajima, Hisakazu; Tsumura, Kumi; Kizaki, Zenro; Oka, Akira; Ogata, Tsutomu; Fukami, Maki; Kagami, Masayo.
Afiliação
  • Inoue T; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, 2-10-1, Okura Setagaya-ku, Tokyo, 157-8535 Japan.
  • Nakamura A; Department of Pediatrics, The University of Tokyo Hospital, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655 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.
  • Sano S; 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 Molecular Endocrinology, National Research Institute for Child Health and Development, 2-10-1, Okura Setagaya-ku, Tokyo, 157-8535 Japan.
  • Mizuno S; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, 2-10-1, Okura Setagaya-ku, Tokyo, 157-8535 Japan.
  • Matsukura Y; Department of Pediatrics, Central Hospital, Aichi Human Service Center, 713-8 Kagiya-cho, Kasugai, Aichi 480-0392 Japan.
  • Harashima C; Department of Pediatrics, The Japan Baptist Hospital, 47 Yamanomoto-cho, Kitashirakawa, Sakyo-ku, Kyoto, 606-8273 Japan.
  • Hasegawa T; Department of Pediatrics, The Japan Baptist Hospital, 47 Yamanomoto-cho, Kitashirakawa, Sakyo-ku, Kyoto, 606-8273 Japan.
  • Nakajima H; Department of Pediatrics, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kamigyo-ku, Kyoto, 602-8566 Japan.
  • Tsumura K; Department of Pediatrics, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kamigyo-ku, Kyoto, 602-8566 Japan.
  • Kizaki Z; Tsumura Family Clinic, Kumi Shounika, 858-1 Watarihashi-cho, Izumo, Shimane 693-0004 Japan.
  • Oka A; Department of Pediatrics, Japanese Red Cross Kyoto Daiichi Hospital, 15-749 Honmachi Higashiyama-ku, Kyoto, 605-0981 Japan.
  • Ogata T; Department of Pediatrics, The University of Tokyo Hospital, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655 Japan.
  • Fukami M; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, 2-10-1, Okura Setagaya-ku, Tokyo, 157-8535 Japan.
  • Kagami M; Department of Pediatrics, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-ku, Hamamatsu, Shizuoka 431-3192 Japan.
Clin Epigenetics ; 9: 52, 2017.
Article em En | MEDLINE | ID: mdl-28515796
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Deficiências do Desenvolvimento / Hibridização Genômica Comparativa / Síndrome de Silver-Russell / Variações do Número de Cópias de DNA / Cardiopatias Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Deficiências do Desenvolvimento / Hibridização Genômica Comparativa / Síndrome de Silver-Russell / Variações do Número de Cópias de DNA / Cardiopatias Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article