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MeSH:(Hearing Loss, Sensorineural/genetics*)

2.Genetic and phenotypic analysis of MYO15A rare variants associated with autosomal recessive hearing loss.

Yun LIN ; Jun XU ; Tao YANG

Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2024;38(1):38-43

3.GJB2 (Cx26) gene mutations in Chinese patients with congenital sensorineural deafness and a report of one novel mutation.

Zi-an XIAO ; Ding-hua XIE

Chinese Medical Journal 2004;117(12):1797-1801

6.Genetic counseling for hearing loss today.

Qiuju WANG ; Lin HE

Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2024;38(1):1-7

7.Next-generation sequencing in molecular diagnosis of hereditary hearing loss.

Wan DU ; Yufen GUO

Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2014;28(22):1815-1818

8.The study of GJB2 dominant mutaion distribution in Chinese deafness patient and the analysis of phenotype.

Shasha HUANG ; Bangqing HUANG ; Yongyi YUAN ; Guojian WANG ; Pu DAI

Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2014;28(22):1744-1747

9.Splicing mutations of GSDME cause late-onset non-syndromic hearing loss.

Danyang LI ; Hongyang WANG ; Qiuju WANG

Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2024;38(1):30-37

10.Identification of novel pathogenic variants of TRIOBP gene in a pedigree affected with non-syndromic deafness.

Menglong FENG ; Kai ZHOU ; Lancheng HUANG ; Fengzhu TANG ; Shenhong QU ; Qiutian LU ; Ruichun CHEN ; Fengti LI

Chinese Journal of Medical Genetics 2021;38(5):454-457

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