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BMC Medical Genomics|June 17, 2022
Novel homozygous variant in the PDZD7 gene in a family with nonsyndromic sensorineural hearing lossQiang Du, Qin Sun, Xiaodong Gu, et al.
International Journal of Pediatric Otorhinolaryngology|January 27, 2016
A novel recessive truncating mutation in MYO15A causing prelingual sensorineural hearing lossWei Li, Luo Guo, Yu Li, et al.
International Journal of Pediatric Otorhinolaryngology|April 2, 2015
Novel biallelic OTOGL mutations in a Chinese family with moderate non-syndromic sensorineural hearing lossXiaodong Gu, Shan Sun, Luo Guo, et al.
Clinical and Translational Medicine|September 30, 2022
The heterogeneity of mammalian utricular cells over the course of developmentDan You, Jin Guo, Yunzhong Zhang, et al.
BMC Medical Genomics|March 19, 2024
A novel intronic TCOF1 pathogenic variant in a Chinese family with Treacher Collins syndromeHaojie Sun, Xinda Xu, Binjun Chen, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 19, 2016
Extensive Supporting Cell Proliferation and Mitotic Hair Cell Generation by In Vivo Genetic Reprogramming in the Neonatal Mouse CochleaWenli Ni, Chen Lin, Luo Guo, et al.
Frontiers in Cellular Neuroscience|February 9, 2019
Transduction of Adeno-Associated Virus Vectors Targeting Hair Cells and Supporting Cells in the Neonatal Mouse CochleaXi Gu, Renjie Chai, Luo Guo, et al.
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