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A case of de novo -α3.7 thalassaemia and the utility of CATSA for detecting de novo mutations in thalassaemia.
Zhang, Lei; Chang, Ming; Liu, Chao; Xu, Yong; Feng, Qing; Yin, Shanshan; Wu, Weiqing.
Afiliación
  • Zhang L; Medical Genetics Center, Shenzhen Maternity and Child Healthcare Hospital, Shenzhen, Guangdong, China.
  • Chang M; Department of Hematology, The Seventh Affiliated Hospital of Sun Yat-Sen University, Shenzhen, Guangdong, China.
  • Liu C; Medical Genetics Center, Shenzhen Maternity and Child Healthcare Hospital, Shenzhen, Guangdong, China.
  • Xu Y; Medical Genetics Center, Shenzhen Maternity and Child Healthcare Hospital, Shenzhen, Guangdong, China.
  • Feng Q; Medical Genetics Center, Shenzhen Maternity and Child Healthcare Hospital, Shenzhen, Guangdong, China.
  • Yin S; Medical Genetics Center, Shenzhen Maternity and Child Healthcare Hospital, Shenzhen, Guangdong, China.
  • Wu W; Medical Genetics Center, Shenzhen Maternity and Child Healthcare Hospital, Shenzhen, Guangdong, China.
Br J Haematol ; 2024 May 16.
Article en En | MEDLINE | ID: mdl-38757312

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Br J Haematol Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Br J Haematol Año: 2024 Tipo del documento: Article País de afiliación: China
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