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A comprehensive and universal approach for embryo testing in patients with different genetic disorders.
Zhang, Shuo; Lei, Caixia; Wu, Junping; Xiao, Min; Zhou, Jing; Zhu, Saijuan; Fu, Jing; Lu, Daru; Sun, Xiaoxi; Xu, Congjian.
Afiliación
  • Zhang S; Shanghai Ji Ai Genetics & IVF Institute, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
  • Lei C; Shanghai Ji Ai Genetics & IVF Institute, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
  • Wu J; Shanghai Ji Ai Genetics & IVF Institute, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
  • Xiao M; Shanghai Ji Ai Genetics & IVF Institute, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
  • Zhou J; Shanghai Ji Ai Genetics & IVF Institute, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
  • Zhu S; Shanghai Ji Ai Genetics & IVF Institute, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
  • Fu J; Shanghai Ji Ai Genetics & IVF Institute, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
  • Lu D; State Key Laboratory of Genetic Engineering, School of Life Science, Fudan University, Shanghai, China.
  • Sun X; NHC Key Laboratory of Birth Defects and Reproductive Health, Chongqing Key Laboratory of Birth Defects and Reproductive Health, Chongqing Population and Family Planning, Science and Technology Research Institute, Chongqing, China.
  • Xu C; Shanghai Ji Ai Genetics & IVF Institute, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
Clin Transl Med ; 11(7): e490, 2021 07.
Article en En | MEDLINE | ID: mdl-34323405
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pruebas Genéticas / Enfermedades Genéticas Congénitas Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Clin Transl Med Año: 2021 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
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XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pruebas Genéticas / Enfermedades Genéticas Congénitas Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Clin Transl Med Año: 2021 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos