Your browser doesn't support javascript.
loading
Next-generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss.
Xiang, Yan-Bao; Xu, Chen-Yang; Xu, Yun-Zhi; Li, Huan-Zheng; Zhou, Li-Li; Xu, Xue-Qin; Chen, Zi-Hui; Tang, Shao-Hua.
Afiliação
  • Xiang YB; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China.
  • Xu CY; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China.
  • Xu YZ; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China.
  • Li HZ; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China.
  • Zhou LL; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China.
  • Xu XQ; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China.
  • Chen ZH; Key laboratory of Medical Genetic, School of Laboratory Medicine and Life Science, Wenzhou Medical University, Wenzhou, China.
  • Tang SH; Key Laboratory of Birth Defects, Department of Genetics, Wenzhou Central Hospital, Wenzhou, China.
Mol Genet Genomic Med ; 8(12): e1539, 2020 12.
Article em En | MEDLINE | ID: mdl-33095980
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Surdez / Loci Gênicos / Mutação Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Surdez / Loci Gênicos / Mutação Idioma: En Ano de publicação: 2020 Tipo de documento: Article