2021-12-11
Sat
13:30-15:20
分会场二临床遗传学分会场
临床遗传学分会场（一）
13:30-14:00
遗传性耳聋基因编辑与基因治疗
14:00-14:30
GENETIC DEAFNESS COMMONS: An integrated resource to explore the pathogenesis of hearing loss through Genetics and Genomics
14:30-14:45
Functional analysis of a novel single-base deletion RUNX2 mutation in patient with cleidocranial dysplasia and clinical orthodontic treatment
14:45-15:00
Molecular diagnosis of hepatic glycogen storage diseasesby a custom-designed panel sequencing:Results in 134Chinese patients from a single center
15:00-15:20
多元化基因组检测平台在不同类型临床样本中的灵活应用与分析
