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A new in-frame deletion in ribosomal protein S19 in a Chinese infant with Diamond-Blackfan anemia.
Zhang, Jing-Ying; Jia, Ming; Zhao, Hai-Zhao; Luo, Ze-Bin; Xu, Wei-Qun; Shen, He-Ping; Tang, Yong-Min.
Afiliación
  • Zhang JY; Division of Hematology-Oncology, Children's Hospital of Zhejiang University School of Medicine, Key Laboratory of Reproductive Genetics (Zhejiang University), Ministry of Education, Hangzhou 310003, PR China.
  • Jia M; Division of Hematology-Oncology, Children's Hospital of Zhejiang University School of Medicine, Key Laboratory of Reproductive Genetics (Zhejiang University), Ministry of Education, Hangzhou 310003, PR China.
  • Zhao HZ; Division of Hematology-Oncology, Children's Hospital of Zhejiang University School of Medicine, Key Laboratory of Reproductive Genetics (Zhejiang University), Ministry of Education, Hangzhou 310003, PR China.
  • Luo ZB; Division of Hematology-Oncology, Children's Hospital of Zhejiang University School of Medicine, Key Laboratory of Reproductive Genetics (Zhejiang University), Ministry of Education, Hangzhou 310003, PR China.
  • Xu WQ; Division of Hematology-Oncology, Children's Hospital of Zhejiang University School of Medicine, Key Laboratory of Reproductive Genetics (Zhejiang University), Ministry of Education, Hangzhou 310003, PR China.
  • Shen HP; Division of Hematology-Oncology, Children's Hospital of Zhejiang University School of Medicine, Key Laboratory of Reproductive Genetics (Zhejiang University), Ministry of Education, Hangzhou 310003, PR China.
  • Tang YM; Division of Hematology-Oncology, Children's Hospital of Zhejiang University School of Medicine, Key Laboratory of Reproductive Genetics (Zhejiang University), Ministry of Education, Hangzhou 310003, PR China. Electronic address: y_m_tang@zju.edu.cn.
Blood Cells Mol Dis ; 62: 1-5, 2016 11.
Article en En | MEDLINE | ID: mdl-27732904

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Ribosómicas / Nucléolo Celular / Mutación del Sistema de Lectura / Eliminación de Secuencia / Anemia de Diamond-Blackfan Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Female / Humans / Infant Idioma: En Revista: Blood Cells Mol Dis Asunto de la revista: HEMATOLOGIA Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Ribosómicas / Nucléolo Celular / Mutación del Sistema de Lectura / Eliminación de Secuencia / Anemia de Diamond-Blackfan Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Female / Humans / Infant Idioma: En Revista: Blood Cells Mol Dis Asunto de la revista: HEMATOLOGIA Año: 2016 Tipo del documento: Article