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Case Report: A Novel Heterozygous ZP3 Deletion Associated With Empty Follicle Syndrome and Abnormal Follicular Development.
Chen, Yongzhe; Wang, Zesong; Wu, Yueren; He, Wenbin; Du, Juan; Cai, Sufen; Gong, Fei; Lu, Guangxiu; Lin, Ge; Dai, Can.
Afiliação
  • Chen Y; School of Basic Medical Science, Central South University, Changsha, China.
  • Wang Z; National Health Commission Key Laboratory of Human Stem Cell and Reproductive Engineering, Central South University, Changsha, China.
  • Wu Y; Department of Basic Medicine, School of Medicine, Hunan Normal University, Changsha, China.
  • He W; Department of Basic Medicine, School of Medicine, Hunan Normal University, Changsha, China.
  • Du J; Reproductive and Genetic Hospital of China International Trust Investment Corporation Xiangya, Changsha, China.
  • Cai S; Clinical Research Center for Reproduction and Genetics in Hunan Province, Changsha, China.
  • Gong F; School of Basic Medical Science, Central South University, Changsha, China.
  • Lu G; National Health Commission Key Laboratory of Human Stem Cell and Reproductive Engineering, Central South University, Changsha, China.
  • Lin G; Reproductive and Genetic Hospital of China International Trust Investment Corporation Xiangya, Changsha, China.
  • Dai C; Clinical Research Center for Reproduction and Genetics in Hunan Province, Changsha, China.
Front Genet ; 12: 690070, 2021.
Article em En | MEDLINE | ID: mdl-34093671
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Genet Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Genet Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China