Last Posted: Jan 31, 2019
- Mutation screening in non-syndromic hearing loss patients with cochlear implantation by massive parallel sequencing in Taiwan.
Liu Wei-Hsiu et al. PloS one 2019 14(1) e0211261 - Gene mutation analysis and genetic counseling for patients with non-syndromic hearing loss in Linyi region.
Li Huafeng et al. Experimental and therapeutic medicine 2019 Jan 17(1) 413-417 - Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group.
Kashtan Clifford E et al. Kidney international 2018 93(5) 1045-1051 - Effect of Genetically Low 25-Hydroxyvitamin D on Mortality Risk: Mendelian Randomization Analysis in 3 Large European Cohorts.
Aspelund Thor et al. Nutrients 2019 Jan 11(1) - Genetics of Usher Syndrome: New Insights From a Meta-analysis.
Jouret Guillaume et al. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2019 Jan 40(1) 121-129 - Rapid and Reliable Detection of Nonsyndromic Hearing Loss Mutations by Multicolor Melting Curve Analysis.
Wang Xudong et al. Scientific reports 2017 742894 - Reproductive guidance through prenatal diagnosis and genetic counseling for recessive hereditary hearing loss in high-risk families.
Deng Yuyuan et al. International journal of pediatric otorhinolaryngology 2018 Dec 115114-119 - Generalizing polygenic risk scores from Europeans to Hispanics/Latinos.
Grinde Kelsey E et al. Genetic epidemiology 2018 Oct - [Screening for hotspot mutations associated with genetic hearing impairment in pregnant women and subsequent prenatal diagnosis in high risk pregnancies].
Yang K et al. Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery 2018 Sep 53(9) 645-649 - Analysis of mutation spectrum of common deafness-causing genes in Hakka newborns in southern China by semiconductor sequencing.
Zhao Pingsen et al. Medicine 2018 Sep 97(38) e12285
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