Your browser doesn't support javascript.
loading
Two families with TET3-related disorder showing neurodevelopmental delay with craniofacial dysmorphisms.
Seyama, Rie; Tsuchida, Naomi; Okada, Yasuyuki; Sakata, Sonoko; Hamada, Keisuke; Azuma, Yoshiteru; Hamanaka, Kohei; Fujita, Atsushi; Koshimizu, Eriko; Miyatake, Satoko; Mizuguchi, Takeshi; Makino, Shintaro; Itakura, Atsuo; Okada, Satoshi; Okamoto, Nobuhiko; Ogata, Kazuhiro; Uchiyama, Yuri; Matsumoto, Naomichi.
  • Seyama R; Department of Human Genetics, Yokohama City University, Yokohama, Japan.
  • Tsuchida N; Department of Obstetrics and Gynecology, Juntendo University, Tokyo, Japan.
  • Okada Y; Department of Human Genetics, Yokohama City University, Yokohama, Japan.
  • Sakata S; Department of Rare Disease Genomics, Yokohama City University Hospital, Yokohama, Japan.
  • Hamada K; Department of Pediatrics, National Hospital Organization Higashihiroshima Medical Center, Higashihiroshima, Japan.
  • Azuma Y; Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences, Hiroshima, Japan.
  • Hamanaka K; Department of Biochemistry, Yokohama City University, Yokohama, Japan.
  • Fujita A; Department of Human Genetics, Yokohama City University, Yokohama, Japan.
  • Koshimizu E; Department of Pediatrics, Aichi Medical University, Nagakute, Japan.
  • Miyatake S; Department of Human Genetics, Yokohama City University, Yokohama, Japan.
  • Mizuguchi T; Department of Human Genetics, Yokohama City University, Yokohama, Japan.
  • Makino S; Department of Human Genetics, Yokohama City University, Yokohama, Japan.
  • Itakura A; Department of Human Genetics, Yokohama City University, Yokohama, Japan.
  • Okada S; Department of Human Genetics, Yokohama City University, Yokohama, Japan.
  • Okamoto N; Department of Obstetrics and Gynecology, Juntendo University Urayasu Hospital, Chiba, Japan.
  • Ogata K; Department of Obstetrics and Gynecology, Juntendo University, Tokyo, Japan.
  • Uchiyama Y; Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences, Hiroshima, Japan.
  • Matsumoto N; Department of Medical Genetics, Osaka Women's and Children's Hospital, Osaka, Japan.
J Hum Genet ; 67(3): 157-164, 2022 Mar.
Article en En | MEDLINE | ID: mdl-34719681
Asunto(s)
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anomalías Craneofaciales / Dioxigenasas / Discapacidad Intelectual Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anomalías Craneofaciales / Dioxigenasas / Discapacidad Intelectual Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article