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Clinical, cytogenetic, and molecular analyses of 17 neonates with transient abnormal myelopoiesis and nonconstitutional trisomy 21.
Yuzawa, Kentaro; Terui, Kiminori; Toki, Tsutomu; Kanezaki, Rika; Kobayashi, Akie; Sato, Tomohiko; Kamio, Takuya; Kudo, Ko; Sasaki, Shinya; Endo, Mikiya; Ozono, Shuichi; Nomura, Keiko; Ito, Etsuro.
Afiliação
  • Yuzawa K; Department of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
  • Terui K; Department of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
  • Toki T; Department of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
  • Kanezaki R; Department of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
  • Kobayashi A; Department of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
  • Sato T; Department of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
  • Kamio T; Department of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
  • Kudo K; Department of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
  • Sasaki S; Department of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
  • Endo M; Department of Pediatrics, Iwate Medical University, Morioka, Japan.
  • Ozono S; Department of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.
  • Nomura K; Department of Pediatrics, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan.
  • Ito E; Department of Pediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Pediatr Blood Cancer ; 67(4): e28188, 2020 04.
Article em En | MEDLINE | ID: mdl-32020774
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 21 / Síndrome de Down / Mielopoese / Fator de Transcrição GATA1 / Mutação Limite: Female / Humans / Infant / Male / Newborn Idioma: En Revista: Pediatr Blood Cancer Assunto da revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão
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 / Mielopoese / Fator de Transcrição GATA1 / Mutação Limite: Female / Humans / Infant / Male / Newborn Idioma: En Revista: Pediatr Blood Cancer Assunto da revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão