Article
[Analysis of genetic variation in patients with Waardenburg syndrome type Ⅱ by next generation sequencing].
Zhonghua yi xue za zhi - 24 Mar 2020
Ren S M, Kong X D, Wu Q H, Jiao Z H, Chen C, Qin Z B
Abstract excerpt
Objective: To detect gene mutation sassociated with deafness in four Waardenburg syndrome (WS) type Ⅱ patients, and to explore the possible mechanism of molecular genetics. Methods: All patients with WS were identified at the genetic and prenatal diagnosis center of the First Affiliated Hospital of Zhengzhou University from August 2015 to December 2018.Clinical materials and peripheral blood were collected from...
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