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Copy number variation-associated lncRNAs may contribute to the etiologies of congenital heart disease.
Lu, Yibo; Fang, Qing; Qi, Ming; Li, Xiaoliang; Zhang, Xingyu; Lin, Yuwan; Xiang, Ying; Fu, Qihua; Wang, Bo.
  • Lu Y; Pediatric Translational Medicine Institute, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
  • Fang Q; Pediatric Translational Medicine Institute, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
  • Qi M; Pediatric Translational Medicine Institute, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
  • Li X; Department of Medical Genetics and Molecular Diagnostic Laboratory, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
  • Zhang X; Pediatric Translational Medicine Institute, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
  • Lin Y; Pediatric Translational Medicine Institute, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
  • Xiang Y; Pediatric Translational Medicine Institute, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China. 1262975038@qq.com.
  • Fu Q; Shanghai Key Laboratory of Clinical Molecular Diagnostics for Pediatrics, Shanghai, China. 1262975038@qq.com.
  • Wang B; Pediatric Translational Medicine Institute, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China. qfu@shsmu.edu.cn.
Commun Biol ; 6(1): 189, 2023 02 17.
Article en En | MEDLINE | ID: mdl-36806749

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ARN Largo no Codificante / Cardiopatías Congénitas Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ARN Largo no Codificante / Cardiopatías Congénitas Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article