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[Variation analysis of genes associated with Usher syndrome type 1 in 136 Chinese deafness families].
Ren, S M; Wu, Q H; Chen, Y B; Jiao, Z H; Kong, X D.
Affiliation
  • Ren SM; Genetic and Prenatal Diagnosis Center, Department of Obstetrics and Gynecology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
  • Wu QH; Genetic and Prenatal Diagnosis Center, Department of Obstetrics and Gynecology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
  • Chen YB; Genetic and Prenatal Diagnosis Center, Department of Obstetrics and Gynecology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
  • Jiao ZH; Genetic and Prenatal Diagnosis Center, Department of Obstetrics and Gynecology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
  • Kong XD; Genetic and Prenatal Diagnosis Center, Department of Obstetrics and Gynecology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Article in Zh | MEDLINE | ID: mdl-33730806

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Deafness / Usher Syndromes Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Country/Region as subject: Asia Language: Zh Journal: Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi Year: 2021 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Deafness / Usher Syndromes Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Country/Region as subject: Asia Language: Zh Journal: Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi Year: 2021 Document type: Article Affiliation country: Country of publication: