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- [31] Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing lossJOURNAL OF HUMAN GENETICS, 2017, 62 (02) : 317 - 320Cai, Xin Zhang论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Otolaryngol Head & Neck Surg, Changsha, Hunan, Peoples R China Cent South Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Otolaryngol Head & Neck Surg, Changsha, Hunan, Peoples R ChinaLi, Ying论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Otolaryngol Head & Neck Surg, Changsha, Hunan, Peoples R ChinaXia, Lu论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Otolaryngol Head & Neck Surg, Changsha, Hunan, Peoples R ChinaPeng, Yu论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Otolaryngol Head & Neck Surg, Changsha, Hunan, Peoples R ChinaHe, Chu Feng论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Otolaryngol Head & Neck Surg, Changsha, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Otolaryngol Head & Neck Surg, Changsha, Hunan, Peoples R ChinaJiang, Lu论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Otolaryngol Head & Neck Surg, Changsha, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Otolaryngol Head & Neck Surg, Changsha, Hunan, Peoples R ChinaFeng, Yong论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Otolaryngol Head & Neck Surg, Changsha, Hunan, Peoples R China Cent South Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Otolaryngol Head & Neck Surg, Changsha, Hunan, Peoples R ChinaXia, Kun论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Cent South Univ, Sch Biol Sci & Technol, Changsha, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Otolaryngol Head & Neck Surg, Changsha, Hunan, Peoples R ChinaLiu, Xue Zhong论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Otolaryngol Head & Neck Surg, Leonard M Miller Sch Med, Miami, FL 33136 USA Cent South Univ, Xiangya Hosp, Dept Otolaryngol Head & Neck Surg, Changsha, Hunan, Peoples R ChinaMei, Ling Yun论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Otolaryngol Head & Neck Surg, Changsha, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Otolaryngol Head & Neck Surg, Changsha, Hunan, Peoples R ChinaHu, Zheng Mao论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, State Key Lab Med Genet, 110 Xiangya Rd, Changsha 410078, Hunan, Peoples R China Cent South Univ, Sch Biol Sci & Technol, Changsha, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Otolaryngol Head & Neck Surg, Changsha, Hunan, Peoples R China
- [32] MPZL2 variant analysis with whole exome sequencing in a cohort of Chinese hearing loss patientsINTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2023, 171Li, Weitao论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, ENT Inst, Shanghai 200031, Peoples R China Fudan Univ, Dept Otorhinolaryngol, Eye & ENT Hosp, State Key Lab Med Neurobiol, Shanghai 200031, Peoples R China Fudan Univ, MOE Frontiers Ctr Brain Sci, Shanghai 200031, Peoples R China Fudan Univ, NHC Key Lab Hearing Med, Shanghai 200031, Peoples R China Fudan Univ, ENT Inst, Shanghai 200031, Peoples R ChinaGuo, Luo论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, ENT Inst, Shanghai 200031, Peoples R China Fudan Univ, Dept Otorhinolaryngol, Eye & ENT Hosp, State Key Lab Med Neurobiol, Shanghai 200031, Peoples R China Fudan Univ, MOE Frontiers Ctr Brain Sci, Shanghai 200031, Peoples R China Fudan Univ, NHC Key Lab Hearing Med, Shanghai 200031, Peoples R China Fudan Univ, ENT Inst, Shanghai 200031, Peoples R ChinaChen, Bing论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, ENT Inst, Shanghai 200031, Peoples R China Fudan Univ, Dept Otorhinolaryngol, Eye & ENT Hosp, State Key Lab Med Neurobiol, Shanghai 200031, Peoples R China Fudan Univ, MOE Frontiers Ctr Brain Sci, Shanghai 200031, Peoples R China Fudan Univ, Inst Biomed Sci, Shanghai 200032, Peoples R China Fudan Univ, NHC Key Lab Hearing Med, Shanghai 200031, Peoples R China Fudan Univ, ENT Inst, Shanghai 200031, Peoples R ChinaShu, Yilai论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, ENT Inst, Shanghai 200031, Peoples R China Fudan Univ, Dept Otorhinolaryngol, Eye & ENT Hosp, State Key Lab Med Neurobiol, Shanghai 200031, Peoples R China Fudan Univ, MOE Frontiers Ctr Brain Sci, Shanghai 200031, Peoples R China Fudan Univ, Inst Biomed Sci, Shanghai 200032, Peoples R China Fudan Univ, NHC Key Lab Hearing Med, Shanghai 200031, Peoples R China Fudan Univ, ENT Inst, Shanghai 200031, Peoples R ChinaLi, Huawei论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, ENT Inst, Shanghai 200031, Peoples R China Fudan Univ, Dept Otorhinolaryngol, Eye & ENT Hosp, State Key Lab Med Neurobiol, Shanghai 200031, Peoples R China Fudan Univ, MOE Frontiers Ctr Brain Sci, Shanghai 200031, Peoples R China Fudan Univ, Inst Biomed Sci, Shanghai 200032, Peoples R China Fudan Univ, NHC Key Lab Hearing Med, Shanghai 200031, Peoples R China Fudan Univ, Inst Brain Sci, Shanghai 200032, Peoples R China Fudan Univ, Collaborat Innovat Ctr Brain Sci, Shanghai 200032, Peoples R China Fudan Univ, ENT Inst, Shanghai 200031, Peoples R China
- [33] whole-exome sequencing in patients with syndromic short stature of unknown causeHORMONE RESEARCH IN PAEDIATRICS, 2023, 96 (SUPPL 2): : 112 - 112Dateki, Sumito论文数: 0 引用数: 0 h-index: 0机构: Nagasaki Univ, Grad Sch Biomed Sci, Dept Pediat, Nagasaki, Japan Nagasaki Univ, Grad Sch Biomed Sci, Dept Pediat, Nagasaki, JapanMotokawa, Midori论文数: 0 引用数: 0 h-index: 0机构: Nagasaki Univ Hosp, Dept Pediat, Nagasaki, Japan Nagasaki Univ, Grad Sch Biomed Sci, Dept Pediat, Nagasaki, JapanKawamura, Haruka论文数: 0 引用数: 0 h-index: 0机构: Nagasaki Univ Hosp, Dept Pediat, Nagasaki, Japan Nagasaki Univ, Grad Sch Biomed Sci, Dept Pediat, Nagasaki, JapanHaraguchi, Kohei论文数: 0 引用数: 0 h-index: 0机构: Nagasaki Univ Hosp, Dept Pediat, Nagasaki, Japan Nagasaki Univ, Grad Sch Biomed Sci, Dept Pediat, Nagasaki, JapanShirakawa, Toshihiko论文数: 0 引用数: 0 h-index: 0机构: Nagasaki Univ Hosp, Dept Pediat, Nagasaki, Japan Nagasaki Univ, Grad Sch Biomed Sci, Dept Pediat, Nagasaki, JapanMishima, Hiroyuki论文数: 0 引用数: 0 h-index: 0机构: Nagasaki Univ, Dept Human Genet, Grad Sch Biomed Sci, Nagasaki, Japan Nagasaki Univ, Grad Sch Biomed Sci, Dept Pediat, Nagasaki, JapanYoshiura, Koh-ichiro论文数: 0 引用数: 0 h-index: 0机构: Nagasaki Univ, Dept Human Genet, Grad Sch Biomed Sci, Nagasaki, Japan Nagasaki Univ, Grad Sch Biomed Sci, Dept Pediat, Nagasaki, Japan论文数: 引用数: h-index:机构:
- [34] Value of whole exome sequencing for syndromic retinal dystrophy diagnosis in young patientsCLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2015, 43 (02): : 132 - 138Prokudin, Ivan论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Westmead, Eye & Dev Genet Res Grp, Sydney, NSW 2145, Australia Childrens Med Res Inst, Eye Genet Grp, Sydney, NSW, Australia Childrens Hosp Westmead, Eye & Dev Genet Res Grp, Sydney, NSW 2145, AustraliaLi, Dong论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Ctr Appl Gen, Philadelphia, PA 19104 USA Childrens Hosp Westmead, Eye & Dev Genet Res Grp, Sydney, NSW 2145, AustraliaHe, Sijie论文数: 0 引用数: 0 h-index: 0机构: Univ Chinese Acad Sci, BGI Shenzhen, Shenzhen, Peoples R China Univ Chinese Acad Sci, BGI Educ Ctr, Shenzhen, Peoples R China Childrens Hosp Westmead, Eye & Dev Genet Res Grp, Sydney, NSW 2145, AustraliaGuo, Yiran论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Ctr Appl Gen, Philadelphia, PA 19104 USA Childrens Hosp Westmead, Eye & Dev Genet Res Grp, Sydney, NSW 2145, AustraliaGoodwin, Linda论文数: 0 引用数: 0 h-index: 0机构: Nepean Hosp, Dept Clin Genet, Sydney, NSW, Australia Childrens Hosp Westmead, Eye & Dev Genet Res Grp, Sydney, NSW 2145, AustraliaWilson, Meredith论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Westmead, Dept Clin Genet, Sydney, NSW 2145, Australia Childrens Hosp Westmead, Eye & Dev Genet Res Grp, Sydney, NSW 2145, AustraliaRose, Loreto论文数: 0 引用数: 0 h-index: 0机构: Macquarie Univ, Macquarie Univ Hosp, Ophthalmol Dept, Sydney, NSW 2109, Australia Childrens Hosp Westmead, Eye & Dev Genet Res Grp, Sydney, NSW 2145, AustraliaTian, Lifeng论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Ctr Appl Gen, Philadelphia, PA 19104 USA Childrens Hosp Westmead, Eye & Dev Genet Res Grp, Sydney, NSW 2145, AustraliaChen, Yulan论文数: 0 引用数: 0 h-index: 0机构: Univ Chinese Acad Sci, BGI Shenzhen, Shenzhen, Peoples R China Childrens Hosp Westmead, Eye & Dev Genet Res Grp, Sydney, NSW 2145, AustraliaLiang, Jinlong论文数: 0 引用数: 0 h-index: 0机构: Univ Chinese Acad Sci, BGI Educ Ctr, Shenzhen, Peoples R China Childrens Hosp Westmead, Eye & Dev Genet Res Grp, Sydney, NSW 2145, AustraliaKeating, Brendan论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Univ Penn, Perelman Sch Med, Dept Pediat, Philadelphia, PA 19104 USA Childrens Hosp Westmead, Eye & Dev Genet Res Grp, Sydney, NSW 2145, AustraliaXu, Xun论文数: 0 引用数: 0 h-index: 0机构: Univ Chinese Acad Sci, BGI Shenzhen, Shenzhen, Peoples R China Childrens Hosp Westmead, Eye & Dev Genet Res Grp, Sydney, NSW 2145, AustraliaJamieson, Robyn V.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Westmead, Eye & Dev Genet Res Grp, Sydney, NSW 2145, Australia Univ Sydney, Discipline Ophthalmol, Sydney, NSW 2006, Australia Univ Sydney, Save Sight Inst, Sydney, NSW 2006, Australia Univ Sydney, Discipline Paediat & Child Hlth, Sydney, NSW 2006, Australia Univ Sydney, Discipline Genet Med, Sydney, NSW 2006, Australia Childrens Med Res Inst, Eye Genet Grp, Sydney, NSW, Australia Childrens Hosp Westmead, Eye & Dev Genet Res Grp, Sydney, NSW 2145, AustraliaHakonarson, Hakon论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Univ Penn, Perelman Sch Med, Dept Pediat, Philadelphia, PA 19104 USA Childrens Hosp Westmead, Eye & Dev Genet Res Grp, Sydney, NSW 2145, Australia
- [35] Clinical relevance of targeted exome sequencing in patients with rare syndromic short statureOrphanet Journal of Rare Diseases, 16Gilyazetdinov Kamil论文数: 0 引用数: 0 h-index: 0机构: National Children’s Medical Center,Department of PediatricsJu Young Yoon论文数: 0 引用数: 0 h-index: 0机构: National Children’s Medical Center,Department of PediatricsSukdong Yoo论文数: 0 引用数: 0 h-index: 0机构: National Children’s Medical Center,Department of PediatricsChong Kun Cheon论文数: 0 引用数: 0 h-index: 0机构: National Children’s Medical Center,Department of Pediatrics
- [36] Clinical relevance of targeted exome sequencing in patients with rare syndromic short statureORPHANET JOURNAL OF RARE DISEASES, 2021, 16 (01)Kamil, Gilyazetdinov论文数: 0 引用数: 0 h-index: 0机构: Natl Childrens Med Ctr, Dept Pediat, Tashkent, Uzbekistan Pusan Natl Univ, Res Inst Convergence Biomed Sci & Technol, Yangsan Hosp, Yangsan, South Korea Natl Childrens Med Ctr, Dept Pediat, Tashkent, Uzbekistan论文数: 引用数: h-index:机构:Yoo, Sukdong论文数: 0 引用数: 0 h-index: 0机构: Pusan Natl Univ, Dept Pediat, Div Pediat Endocrinol, Childrens Hosp, Yangsan, South Korea Natl Childrens Med Ctr, Dept Pediat, Tashkent, Uzbekistan论文数: 引用数: h-index:机构:
- [37] Targeted exome sequencing analysis in Turkish non-syndromic craniosynostosis patientsEUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 101 - 102论文数: 引用数: h-index:机构:Nur, B.论文数: 0 引用数: 0 h-index: 0机构: Akdeniz Univ, Antalya, Turkey Akdeniz Univ, Antalya, Turkey论文数: 引用数: h-index:机构:Alper, O. M.论文数: 0 引用数: 0 h-index: 0机构: Akdeniz Univ, Antalya, Turkey Akdeniz Univ, Antalya, Turkey
- [38] Myosin Mutations and Sudden Sensorineural Hearing Loss: Results of Whole Exome SequencingOTOLOGY & NEUROTOLOGY, 2023, 44 (01) : 16 - 20Sharma, Rahul K.论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Otolaryngol Head & Neck Surg, Irving Med Ctr, New York, NY 10032 USA Columbia Univ, Vagelos Coll Phys & Surg, New York, NY USA Columbia Univ, Dept Otolaryngol Head & Neck Surg, Irving Med Ctr, New York, NY 10032 USADrusin, Madeleine论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Otolaryngol Head & Neck Surg, Irving Med Ctr, New York, NY 10032 USA Columbia Univ, Dept Otolaryngol Head & Neck Surg, Irving Med Ctr, New York, NY 10032 USAHostyk, Joseph论文数: 0 引用数: 0 h-index: 0机构: Columba Univ, Inst Genom Med, Irving Med Ctr, New York, NY 10032 USA Columbia Univ, Dept Otolaryngol Head & Neck Surg, Irving Med Ctr, New York, NY 10032 USABaugh, Evan H.论文数: 0 引用数: 0 h-index: 0机构: Columba Univ, Inst Genom Med, Irving Med Ctr, New York, NY 10032 USA Columbia Univ, Dept Otolaryngol Head & Neck Surg, Irving Med Ctr, New York, NY 10032 USAAggarwal, Vimla S.论文数: 0 引用数: 0 h-index: 0机构: Columba Univ, Inst Genom Med, Irving Med Ctr, New York, NY 10032 USA Columbia Univ, Dept Otolaryngol Head & Neck Surg, Irving Med Ctr, New York, NY 10032 USAGoldstein, David论文数: 0 引用数: 0 h-index: 0机构: Columba Univ, Inst Genom Med, Irving Med Ctr, New York, NY 10032 USA Columbia Univ, Dept Otolaryngol Head & Neck Surg, Irving Med Ctr, New York, NY 10032 USAKim, Ana H.论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Otolaryngol Head & Neck Surg, Irving Med Ctr, New York, NY 10032 USA Columbia Univ, Dept Otolaryngol Head & Neck Surg, NewYork Presbyterian, Irving Med Ctr, 180 Ft Washington Ave, HP8-864, New York, NY 10032 USA Columbia Univ, Dept Otolaryngol Head & Neck Surg, Irving Med Ctr, New York, NY 10032 USA
- [39] Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing lossGENETICS IN MEDICINE, 2018, 20 (12) : 1663 - 1676Sheppard, Sarah论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USABiswas, Sawona论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Dept Pathol & Lab Med, Perelman Sch Med, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Div Genom Diagnost, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USALi, Mindy H.论文数: 0 引用数: 0 h-index: 0机构: Rush Univ, Med Ctr, Dept Pediat, Div Genet, Chicago, IL 60612 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USAJayaraman, Vijayakumar论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USASlack, Ian论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USARomasko, Edward J.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Dept Pathol & Lab Med, Perelman Sch Med, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Div Genom Diagnost, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USASasson, Ariella论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Dept Biomed & Hlth Informat, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USABrunton, Joshua论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USARajagopalan, Ramakrishnan论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Dept Pathol & Lab Med, Perelman Sch Med, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Div Genom Diagnost, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Dept Biomed & Hlth Informat, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USASarmady, Mahdi论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Dept Pathol & Lab Med, Perelman Sch Med, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Div Genom Diagnost, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Dept Biomed & Hlth Informat, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USAAbrudan, Jenica L.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USAJairam, Sowmya论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Dept Pathol & Lab Med, Perelman Sch Med, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Div Genom Diagnost, Philadelphia, PA 19104 USA Mem Sloan Kettering Canc Ctr, Dept Pathol, 1275 York Ave, New York, NY 10021 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USADeChene, Elizabeth T.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Genom Diagnost, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USAYing, Xiahoan论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USAChoi, Jiwon论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USAWilkens, Alisha论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Div Genom Diagnost, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USARaible, Sarah E.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USAScarano, Maria I.论文数: 0 引用数: 0 h-index: 0机构: Cooper Univ Hlth Care, Div Genet, Camden, NY USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USASantani, Avni论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Dept Pathol & Lab Med, Perelman Sch Med, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Div Genom Diagnost, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USAPennington, Jeffrey W.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Dept Biomed & Hlth Informat, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USALuo, Minjie论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Dept Pathol & Lab Med, Perelman Sch Med, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Div Genom Diagnost, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USAConlin, Laura K.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Dept Pathol & Lab Med, Perelman Sch Med, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Div Genom Diagnost, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USADevkota, Batsal论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Dept Biomed & Hlth Informat, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USADulik, Matthew C.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Dept Pathol & Lab Med, Perelman Sch Med, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Div Genom Diagnost, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USASpinner, Nancy B.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Dept Pathol & Lab Med, Perelman Sch Med, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Div Genom Diagnost, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USAKrantz, Ian D.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USA
- [40] Mutation screening in non-syndromic hearing loss patients with cochlear implantation by massive parallel sequencing in TaiwanPLOS ONE, 2019, 14 (01):Liu, Wei-Hsiu论文数: 0 引用数: 0 h-index: 0机构: Chang Gung Univ, Dept Lab Med, Chang Gung Mem Hosp, Linkou Branch,Coll Med, Taoyuan, Taiwan Chang Gung Univ, Dept Otolaryngol Head & Neck Surg, Chang Gung Mem Hosp, Linkou Branch,Coll Med, Taoyuan, Taiwan Chang Gung Univ, Dept Lab Med, Chang Gung Mem Hosp, Linkou Branch,Coll Med, Taoyuan, TaiwanChang, Pi-Yueh论文数: 0 引用数: 0 h-index: 0机构: Chang Gung Univ, Dept Med Biotechnol & Lab Sci, Taoyuan, Taiwan Chang Gung Univ, Dept Med Res, Chang Gung Mem Hosp, Taoyuan, Taiwan Chang Gung Univ, Grad Inst Clin Med Sci, Taoyuan, Taiwan Chang Gung Univ, Dept Lab Med, Chang Gung Mem Hosp, Linkou Branch,Coll Med, Taoyuan, TaiwanChang, Shih-Cheng论文数: 0 引用数: 0 h-index: 0机构: Chang Gung Univ, Dept Med Biotechnol & Lab Sci, Taoyuan, Taiwan Chang Gung Univ, Dept Med Res, Chang Gung Mem Hosp, Taoyuan, Taiwan Chang Gung Univ, Grad Inst Clin Med Sci, Taoyuan, Taiwan Chang Gung Univ, Dept Lab Med, Chang Gung Mem Hosp, Linkou Branch,Coll Med, Taoyuan, TaiwanLu, Jang-Jih论文数: 0 引用数: 0 h-index: 0机构: Chang Gung Univ, Dept Med Biotechnol & Lab Sci, Taoyuan, Taiwan Chang Gung Univ, Dept Med Res, Chang Gung Mem Hosp, Taoyuan, Taiwan Chang Gung Univ, Grad Inst Clin Med Sci, Taoyuan, Taiwan Chang Gung Univ, Dept Lab Med, Chang Gung Mem Hosp, Linkou Branch,Coll Med, Taoyuan, TaiwanWu, Che-Ming论文数: 0 引用数: 0 h-index: 0机构: Chang Gung Univ, Dept Otolaryngol Head & Neck Surg, Chang Gung Mem Hosp, Linkou Branch,Coll Med, Taoyuan, Taiwan Chang Gung Univ, Dept Lab Med, Chang Gung Mem Hosp, Linkou Branch,Coll Med, Taoyuan, Taiwan