Genetic etiology study of four Chinese families with two nonsyndromic deaf children in succession by targeted next‐generation sequencing

Author:

Xiao Caixia1ORCID,Liu Shuang1,Wang Hongyue1,Ding Yibing1,Chen Yaqiu1ORCID,Liu Haiyan1

Affiliation:

1. Tianjin Women and Children Healthcare Center Tianjin China

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Reference66 articles.

1. SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations

2. CT and MRI findings in X‐linked progressive deafness;Altay H.;Diagn Interv Radiol,2008

3. Position state Ment 2002;American Academy of Pediatrics Joint Committee on Infant hearing;Pediatrics

4. Targeted next generation sequencing for molecular diagnosis of Usher syndrome;Aparisi M. J.;Orphanet Journal of Rare Diseases,2014

5. Homozygosity for the V37I Connexin 26 mutation in three unrelated children with sensorineural hearing loss

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