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Exploration of the role of gene mutations in myelodysplastic syndromes through a sequencing design involving a small number of target genes.
Xu, Feng; Wu, Ling-Yun; He, Qi; Wu, Dong; Zhang, Zheng; Song, Lu-Xi; Zhao, You-Shan; Su, Ji-Ying; Zhou, Li-Yu; Guo, Juan; Chang, Chun-Kang; Li, Xiao.
Afiliação
  • Xu F; Department of Hematology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
  • Wu LY; Department of Hematology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
  • He Q; Department of Hematology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
  • Wu D; Department of Hematology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
  • Zhang Z; Department of Hematology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
  • Song LX; Department of Hematology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
  • Zhao YS; Department of Hematology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
  • Su JY; Department of Hematology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
  • Zhou LY; Department of Hematology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
  • Guo J; Department of Hematology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
  • Chang CK; Department of Hematology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
  • Li X; Department of Hematology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
Sci Rep ; 7: 43113, 2017 02 21.
Article em En | MEDLINE | ID: mdl-28220884
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Mutação 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: Síndromes Mielodisplásicas / Mutação Idioma: En Ano de publicação: 2017 Tipo de documento: Article