JOURNAL OF SHANDONG UNIVERSITY (OTOLARYNGOLOGY AND OPHTHALMOLOGY)
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HAN Yue-chen, FAN Zhao-min, XU Wei, LI Jian-feng, L〖AKU¨] Zheng-hua, WANG Hai-bo
(Department of Otolaryngology & Head and Neck Surgery, Provincial Hospital Affiliated to Shandong University, Jinan 250021, China
CLC Number:
| [1] | LIU Ruowu, ZHANG Han. Gene therapy for leber hereditary optic neuropathy [J]. Journal of Otolaryngology and Ophthalmology of Shandong University, 2024, 38(4): 154-158. |
| [2] | ZHANG Jin, QI Zhiling, WANG Shaohua, ZHAO Yufeng, MA Xu, WU Yungang. A case report of a new pathogenic gene mutation in neurofibromatosis type I and literature review [J]. Journal of Otolaryngology and Ophthalmology of Shandong University, 2024, 38(2): 73-78. |
| [3] | WEI Hui, ZHANG Mingxi, SUN Yue, XIE Ruxin, CHENG Qiong, LI Linna, XIANG Qianqian, WU Lan, CHEN Zhongshan. Boucher-Neuhäuser syndrome: a case of two siblings with two PNPLA6 mutations and literature review [J]. Journal of Otolaryngology and Ophthalmology of Shandong University, 2023, 37(3): 88-92. |
| [4] | ZHAO Shuang, ZHAO Jun, XUE Youyu, ZHANG Juanmei. Analysis of a new-onset FBN1 gene mutation in a patient with Marfan syndrome [J]. Journal of Otolaryngology and Ophthalmology of Shandong University, 2023, 37(2): 98-103. |
| [5] | ZHUANG Peiyun, LIU Yunyi. Hormones and voice [J]. Journal of Otolaryngology and Ophthalmology of Shandong University, 2021, 35(3): 5-9. |
| [6] | XU Lina, GAO Yanhui, HE Shuangba. Analysis of common deafness genes for hearing loss in Nanjing [J]. Journal of Otolaryngology and Ophthalmology of Shandong University, 2019, 33(6): 45-48. |
| [7] | XU Xinbo, MA Xiaojie, YAN Tao, HAN Xiao, ZHANG Hanbing. A novel PAX3 mutation causing type I Waardenburg syndrome. [J]. JOURNAL OF SHANDONG UNIVERSITY (OTOLARYNGOLOGY AND OPHTHALMOLOGY), 2017, 31(6): 39-41. |
| [8] | SUN Feifei, HU Songqun, TANG Yan, ZHANG Jie, WU Di, QIU Jinhong, WANG Zhixia, ZHANG Luping. A next-generation sequencing gene panel for molecular diagnosis in twelve Chinese families with non-syndromic sensorineural hearing loss. [J]. JOURNAL OF SHANDONG UNIVERSITY (OTOLARYNGOLOGY AND OPHTHALMOLOGY), 2017, 31(5): 45-49. |
| [9] | LIU Shuangshuang, NIU Yuping, SUN Yue, MI Zhaoyuan, SHI Guizhi. Screening analysis of fourteen hereditary deafness gene mutation in patients with Non-syndromic hearing loss in Shandong province. [J]. JOURNAL OF SHANDONG UNIVERSITY (OTOLARYNGOLOGY AND OPHTHALMOLOGY), 2016, 30(4): 63-68. |
| [10] | LI Jian-rui1, LIU Tao1, YAN Jiang-wei2, YANG Ya-ran2, WANG Li-wei3. Mutation analysis of GJB2 in patients with sporadic hearing impairment [J]. JOURNAL OF SHANDONG UNIVERSITY (OTOLARYNGOLOGY AND OPHTHALMOLOGY), 2011, 25(6): 33-36. |
| [11] | LI Jian-rui1, LIU Tao1, YAN Jiang-wei2, YANG Ya-ran2, LI Qi3, DAI Pu4. Molecular genetic analysis of the SLC26A4 IVS7-2A>G mutation in patients with non-syndromic hearing loss [J]. JOURNAL OF SHANDONG UNIVERSITY (OTOLARYNGOLOGY AND OPHTHALMOLOGY), 2011, 25(4): 32-35. |
| [12] | LIU Tao1, BAO Yin2, YAN Jiangwei3, LI Lingxiang1, LI Jianrui4. Molecular genetic analysis of the mtDNA A1555G mutation in patients with nonsyndromic hearing loss [J]. JOURNAL OF SHANDONG UNIVERSITY (OTOLARYNGOLOGY AND OPHTHALMOLOGY), 2009, 23(1): 40-42 . |
| [13] | CHENG Jin-mei,XIE Zhen-yu,LIN Qin,ZHANG Peng-fei,LIN Ying,YI Zi-xiang,TIAN Wei-zhong . Expression and mutation analysis of tumor suppressor PTEN in nasopharyngeal carcinoma [J]. JOURNAL OF SHANDONG UNIVERSITY (OTOLARYNGOLOGY AND OPHTHALMOLOGY), 2008, 22(5): 405-407 . |
| [14] | TIAN Xu,SUN Ming,ZHANG Shuang . [J]. JOURNAL OF SHANDONG UNIVERSITY (OTOLARYNGOLOGY AND OPHTHALMOLOGY), 2006, 20(4): 357-360 . |
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