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Transient myeloproliferative disorder with partial trisomy 21.
Takahashi, Takahide; Inoue, Akira; Yoshimoto, Junko; Kanamitsu, Kiichiro; Taki, Tomohiko; Imada, Masahide; Yamada, Mutsuko; Ninomiya, Shinsuke; Toki, Tsutomu; Terui, Kiminori; Ito, Etsuro; Shimada, Akira.
Afiliação
  • Takahashi T; Division of Medical Support, Okayama University Hospital, Okayama, Japan.
  • Inoue A; Department of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Yoshimoto J; Department of Pediatrics, Okayama University Hospital, Okayama, Japan.
  • Kanamitsu K; Department of Pediatrics, Okayama University Hospital, Okayama, Japan.
  • Taki T; Department of Molecular Diagnostics and Therapeutics, Kyoto Prefectural University of Medicine, Graduate School of Medical Science, Kyoto, Japan.
  • Imada M; Division of Medical Support, Okayama University Hospital, Okayama, Japan.
  • Yamada M; Department of Pediatrics, Okayama University Hospital, Okayama, Japan.
  • Ninomiya S; Department of Clinical Genetics, Kurashiki Central Hospital, Kurashiki, Japan.
  • Toki T; Department of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
  • Terui K; Department of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
  • Ito E; Department of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
  • Shimada A; Department of Pediatrics, Okayama University Hospital, Okayama, Japan.
Pediatr Blood Cancer ; 62(11): 2021-4, 2015 Nov.
Article em En | MEDLINE | ID: mdl-26138905
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 21 / Síndrome de Down / Polimorfismo de Nucleotídeo Único / Transtornos Mieloproliferativos Limite: Female / Humans / Infant Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 21 / Síndrome de Down / Polimorfismo de Nucleotídeo Único / Transtornos Mieloproliferativos Limite: Female / Humans / Infant Idioma: En Ano de publicação: 2015 Tipo de documento: Article