A Summary on hearing and genetic screening of newborn in Hei LongjiangProvince
Abstract：A total of 443 newborns were taken hearing and genetic screening at Harbin Children Hospital during May 2014 to June 2015. And 104 cases had partial gene mutations,including 52 cases of GJB2 gene mutation,50 cases of SLC26A4 gene mutation and 2 of MT-RNR1(12SrRNA)gene mutation. Newborn Hearing and Genetic Screening is of great significance, however,it is still not available to all newborns.
Keywords：Neonatal ScreeningEarly DiagnosisHearingGene
Publication Date：2015-07-02
Online Publishing Date：2025-08-15(First online date of this platform, not the publication date of the document)
Pages：3( 205-207 )