Your browser doesn't support javascript.
loading
A neonatal case of HDR syndrome and a vascular ring with a novel GATA3 mutation.
Kusakawa, Moe; Sato, Takeshi; Hosoda, Ai; Araki, Eriko; Matsuzaki, Yohei; Yamashita, Yukio; Ishihara, Jun; Inagaki, Yoshinori; Uchida, Noboru; Ishii, Tomohiro; Hasegawa, Tomonobu.
Afiliação
  • Kusakawa M; 1Department of Pediatrics, Yokohama Municipal Citizen's Hospital, 56 Okazawa-cho, Hodogaya-ku, Yokohama, Kanagawa Japan.
  • Sato T; 2Department of Pediatrics, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo Japan.
  • Hosoda A; 2Department of Pediatrics, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo Japan.
  • Araki E; 1Department of Pediatrics, Yokohama Municipal Citizen's Hospital, 56 Okazawa-cho, Hodogaya-ku, Yokohama, Kanagawa Japan.
  • Matsuzaki Y; 1Department of Pediatrics, Yokohama Municipal Citizen's Hospital, 56 Okazawa-cho, Hodogaya-ku, Yokohama, Kanagawa Japan.
  • Yamashita Y; 1Department of Pediatrics, Yokohama Municipal Citizen's Hospital, 56 Okazawa-cho, Hodogaya-ku, Yokohama, Kanagawa Japan.
  • Ishihara J; 1Department of Pediatrics, Yokohama Municipal Citizen's Hospital, 56 Okazawa-cho, Hodogaya-ku, Yokohama, Kanagawa Japan.
  • Inagaki Y; 1Department of Pediatrics, Yokohama Municipal Citizen's Hospital, 56 Okazawa-cho, Hodogaya-ku, Yokohama, Kanagawa Japan.
  • Uchida N; 3Department of Neonatology, Kanagawa Children's Medical Center, 2-138-4 Mutsukawa, Minami-ku, Yokohama, Kanagawa Japan.
  • Ishii T; 2Department of Pediatrics, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo Japan.
  • Hasegawa T; 2Department of Pediatrics, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo Japan.
Hum Genome Var ; 6: 55, 2019.
Article em En | MEDLINE | ID: mdl-31885872
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Hum Genome Var Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Hum Genome Var Ano de publicação: 2019 Tipo de documento: Article