Development and validation of a fetal genotyping assay with potential for noninvasive prenatal diagnosis of hereditary hearing loss

Author:

Chen Ying12,Liu Yiqian3,Wang Benjing4,Mao Jun15,Wang Ting6,Ye Kan7,Ye Yanlin7,Cram David S.3,Li Hong6

Affiliation:

1. Central Lab; Suzhou Hospital Affiliated to Nanjing Medical University; Suzhou Jiangsu China

2. Nanjing Medical University Affiliated Wuxi Maternity and Child Health Care Hospital; Wuxi Jiangsu China

3. Berry Genomics Corporation; Beijing China

4. Gynecology Department; Suzhou Hospital Affiliated to Nanjing Medical University; Suzhou Jiangsu China

5. Obstetrics Department; Suzhou Hospital Affiliated to Nanjing Medical University; Suzhou Jiangsu China

6. Center for Reproduction and Genetics; Suzhou Hospital Affiliated to Nanjing Medical University; Suzhou Jiangsu China

7. Child Health Care Department; Suzhou Hospital Affiliated to Nanjing Medical University; Suzhou Jiangsu China

Funder

‘Thirteenth Five’ Key Medical Talent's Project in Science and Education of Jiangsu Province, Jiangsu Provincial Key Discipline Construction Project

Clinical Medicine Science and Technology Projects of Jiangsu Province

Jiangsu Provincial Health Department Scientific Research Project

Suzhou Key Medical Center

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference36 articles.

1. Deafness genes;Kitamura;J Med Dent Sci,2000

2. Molecular genetics of non-syndromic deafness;Piatto;Braz J Otorhinolaryngol,2005

3. Prevalence and etiology of people with hearing impairment in China;Sun;Zhong Hua Liu Xing Bing Xue Za Zhi,2008

4. The genetic bases for non-syndromic hearing loss among Chinese;Ouyang;J Hum Genet,2009

5. Enter the dragon-China's journey to the hearing world;Liang;Cochlear Implants Int,2013

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