[Mutational analysis and prenatal diagnosis of <i>TMPRSS3</i> gene in two Chinese families affected with deafness].

Ren, S M; Wu, Q H; Chen, C; Kong, X D

[Mutational analysis and prenatal diagnosis of TMPRSS3 gene in two Chinese families affected with deafness].

Ren, S M; Wu, Q H; Chen, C; Kong, X D.

Afiliação

Ren SM; Genetic and Prenatal Diagnosis Center of the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Wu QH; Genetic and Prenatal Diagnosis Center of the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Chen C; Genetic and Prenatal Diagnosis Center of the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Kong XD; Genetic and Prenatal Diagnosis Center of the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi ; 55(4): 344-349, 2020 04 07.

Article em Zh | MEDLINE | ID: mdl-32306631

Assuntos

Surdez/diagnóstico; Surdez/genética; Proteínas de Membrana/genética; Proteínas de Neoplasias/genética; Diagnóstico Pré-Natal; Serina Endopeptidases/genética; Análise Mutacional de DNA; Feminino; Heterozigoto; Humanos; Mutação; Linhagem; Gravidez

Palavras-chave

Deafness; Next generation sequencing; Prenatal diagnosis; TMPRSS3

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diagnóstico Pré-Natal / Serina Endopeptidases / Surdez / Proteínas de Membrana / Proteínas de Neoplasias Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Pregnancy Idioma: Zh Revista: Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China

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