Targeted Next-Generation Sequencing in Uyghur Families with Non-Syndromic Sensorineural Hearing Loss

Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients

(2014) D. Vozzi et al.   GENE

Mutation analysis of seven consanguineous Uyghur families with non-syndromic deafness

(2014) Zhen-tao Wang et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY

Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study

(2013) Hideki Mutai et al.   Orphanet Journal of Rare Diseases

Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing

(2013) Tao Yang et al.   Orphanet Journal of Rare Diseases

Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families

(2012) Jeong-In Baek et al.   Orphanet Journal of Rare Diseases

Common Molecular Etiologies Are Rare in Nonsyndromic Tibetan Chinese Patients with Hearing Impairment

(2012) Yongyi Yuan et al.   PLoS One

Genetic mutations in non-syndromic deafness patients of uyghur and han chinese ethnicities in xinjiang, China: a comparative study

(2011) Yu Chen et al.   Journal of Translational Medicine

Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct

(2011) Shasha Huang et al.   Journal of Translational Medicine

Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G,GJB2,andSLC26A4mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China

(2010) Yu-bin Ji et al.   ACTA OTO-LARYNGOLOGICA

Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia

(2009) M Tekin et al.   CLINICAL GENETICS

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

(2009) Pu Dai et al.   Journal of Translational Medicine