Utility of Whole Genome Sequencing for Population Screening of Deafness-Related Genetic Variants and Cytomegalovirus Infection in Newborns.

Xiang, Jiale; Zhang, Hongfu; Sun, Xiangzhong; Zhang, Junqing; Xu, Zhenpeng; Sun, Jun; Peng, Zhiyu

Xiang, Jiale; Zhang, Hongfu; Sun, Xiangzhong; Zhang, Junqing; Xu, Zhenpeng; Sun, Jun; Peng, Zhiyu.

Afiliação

Xiang J; College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China.
Zhang H; BGI Genomics, BGI-Shenzhen, Shenzhen, China.
Sun X; BGI Genomics, BGI-Shenzhen, Shenzhen, China.
Zhang J; BGI Genomics, BGI-Shenzhen, Shenzhen, China.
Xu Z; Tianjin Medical Laboratory, BGI-Tianjin, BGI-Shenzhen, Tianjin, China.
Sun J; BGI-Wuhan Clinical Laboratories, BGI-Shenzhen, Wuhan, China.
Peng Z; Tianjin Medical Laboratory, BGI-Tianjin, BGI-Shenzhen, Tianjin, China.

Front Genet ; 13: 883617, 2022.

Article em En | MEDLINE | ID: mdl-35571039

Palavras-chave

WGS; cytomegalovirus infection; genetic variation; hearing loss; newborns

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Idioma: En Revista: Front Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

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