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- [31] Identification of two novel mutations in three Chinese families with Kallmann syndrome using whole exome sequencingANDROLOGIA, 2020, 52 (07)Zhang, Qin论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Endocrinol, Changsha, Peoples R China Cent South Univ, Dept Endocrinol, Changsha, Peoples R ChinaHe, Hong-hui论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Endocrinol, Changsha, Peoples R China Cent South Univ, Dept Endocrinol, Changsha, Peoples R ChinaJanjua, Muhammad Usman论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Endocrinol, Changsha, Peoples R China Cent South Univ, Dept Endocrinol, Changsha, Peoples R ChinaWang, Fang论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Endocrinol, Changsha, Peoples R China Cent South Univ, Dept Endocrinol, Changsha, Peoples R ChinaYang, You-bo论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Endocrinol, Changsha, Peoples R China Cent South Univ, Dept Endocrinol, Changsha, Peoples R ChinaMo, Zhao-hui论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Endocrinol, Changsha, Peoples R China Cent South Univ, Dept Endocrinol, Changsha, Peoples R ChinaLiu, Jun论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Endocrinol, Changsha, Peoples R China Cent South Univ, Dept Endocrinol, Changsha, Peoples R ChinaJin, Ping论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Dept Endocrinol, Changsha, Peoples R China Cent South Univ, Dept Endocrinol, Changsha, Peoples R China
- [32] Analysis of a Chinese Pedigree With Familial Chylomicronemia Syndrome Reveals Two Novel LPL Mutations by Whole-Exome SequencingFRONTIERS IN GENETICS, 2020, 11Liu, Ying论文数: 0 引用数: 0 h-index: 0机构: Peking Univ, Dept Pediat, Shenzhen Hosp, Shenzhen, Peoples R China Peking Univ, Dept Pediat, Shenzhen Hosp, Shenzhen, Peoples R ChinaLan, Zhangzhang论文数: 0 引用数: 0 h-index: 0机构: Southern Univ Sci & Technol, Sch Med, Shenzhen, Peoples R China Peking Univ, Dept Pediat, Shenzhen Hosp, Shenzhen, Peoples R ChinaZhao, Fang论文数: 0 引用数: 0 h-index: 0机构: Peking Univ, Dept Pediat, Shenzhen Hosp, Shenzhen, Peoples R China Peking Univ, Dept Pediat, Shenzhen Hosp, Shenzhen, Peoples R ChinaZhang, Shuangchuan论文数: 0 引用数: 0 h-index: 0机构: Peking Univ, Dept Pediat, Shenzhen Hosp, Shenzhen, Peoples R China Peking Univ, Dept Pediat, Shenzhen Hosp, Shenzhen, Peoples R ChinaZhang, Wenyong论文数: 0 引用数: 0 h-index: 0机构: Southern Univ Sci & Technol, Sch Med, Shenzhen, Peoples R China Peking Univ, Dept Pediat, Shenzhen Hosp, Shenzhen, Peoples R China
- [33] Whole-exome sequencing identifies two novel ALMS1 mutations in Indian patients with Leber congenital amaurosisHuman Genome Variation, 8Natarajan N. Srikrupa论文数: 0 引用数: 0 h-index: 0机构: Vision Research Foundation,SNONGC Department of Genetics and Molecular BiologySarangapani Sripriya论文数: 0 引用数: 0 h-index: 0机构: Vision Research Foundation,SNONGC Department of Genetics and Molecular BiologySuriyanarayanan Pavithra论文数: 0 引用数: 0 h-index: 0机构: Vision Research Foundation,SNONGC Department of Genetics and Molecular BiologyParveen Sen论文数: 0 引用数: 0 h-index: 0机构: Vision Research Foundation,SNONGC Department of Genetics and Molecular BiologyRavi Gupta论文数: 0 引用数: 0 h-index: 0机构: Vision Research Foundation,SNONGC Department of Genetics and Molecular BiologySinnakaruppan Mathavan论文数: 0 引用数: 0 h-index: 0机构: Vision Research Foundation,SNONGC Department of Genetics and Molecular Biology
- [34] Whole-exome sequencing identifies two novel ALMS1 mutations in Indian patients with Leber congenital amaurosisHUMAN GENOME VARIATION, 2021, 8 (01)Srikrupa, Natarajan N.论文数: 0 引用数: 0 h-index: 0机构: Sankara Nethralaya, Vis Res Fdn, SNONGC Dept Genet & Mol Biol, Chennai, Tamil Nadu, India Sankara Nethralaya, Vis Res Fdn, SNONGC Dept Genet & Mol Biol, Chennai, Tamil Nadu, IndiaSripriya, Sarangapani论文数: 0 引用数: 0 h-index: 0机构: Sankara Nethralaya, Vis Res Fdn, SNONGC Dept Genet & Mol Biol, Chennai, Tamil Nadu, India Sankara Nethralaya, Vis Res Fdn, SNONGC Dept Genet & Mol Biol, Chennai, Tamil Nadu, IndiaPavithra, Suriyanarayanan论文数: 0 引用数: 0 h-index: 0机构: SASTRA, Sch Chem & Biotechnol, Thanjavur, India Sankara Nethralaya, Vis Res Fdn, SNONGC Dept Genet & Mol Biol, Chennai, Tamil Nadu, IndiaSen, Parveen论文数: 0 引用数: 0 h-index: 0机构: Sankara Nethralaya, Med Res Fdn, Shri Bhagwan Mahavir Vitreoretinal Serv, Chennai, India Sankara Nethralaya, Vis Res Fdn, SNONGC Dept Genet & Mol Biol, Chennai, Tamil Nadu, IndiaGupta, Ravi论文数: 0 引用数: 0 h-index: 0机构: MedGenome Labs Pvt Ltd, Bangalore, Karnataka, India Sankara Nethralaya, Vis Res Fdn, SNONGC Dept Genet & Mol Biol, Chennai, Tamil Nadu, IndiaMathavan, Sinnakaruppan论文数: 0 引用数: 0 h-index: 0机构: Sankara Nethralaya, Vis Res Fdn, SNONGC Dept Genet & Mol Biol, Chennai, Tamil Nadu, India Sankara Nethralaya, Vis Res Fdn, SNONGC Dept Genet & Mol Biol, Chennai, Tamil Nadu, India
- [35] Whole-Exome Sequencing Identifies Homozygote Nonsense Variants in LMOD2 Gene Causing Infantile Dilated CardiomyopathyCELLS, 2023, 12 (11)Sono, Reiri论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USALarrinaga, Tania M.论文数: 0 引用数: 0 h-index: 0机构: Univ Arizona, Dept Cellular & Mol Med, Tucson, AZ 85721 USA Univ Arizona, Sarver Mol Cardiovasc Res Program, Tucson, AZ 85721 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USAHuang, Alden论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USAMakhlouf, Frank论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Neonatal Congenital Heart Lab, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USAKang, Xuedong论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Neonatal Congenital Heart Lab, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USASu, Jonathan论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USALau, Ryan论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USAArboleda, Valerie A.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA Univ Calif Los Angeles, Mol Biol Inst, Los Angeles, CA 90095 USA Univ Calif Los Angeles, Eli & Edyth Broad Stem Cell Res Ctr, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USABiniwale, Reshma论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Surg, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USAFishbein, Gregory A.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USAKhanlou, Negar论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USASi, Ming-Sing论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Surg, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USASatou, Gary M.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USAHalnon, Nancy论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USAVan Arsdell, Glen S.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Surg, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USAGregorio, Carol C.论文数: 0 引用数: 0 h-index: 0机构: Univ Arizona, Dept Cellular & Mol Med, Tucson, AZ 85721 USA Univ Arizona, Sarver Mol Cardiovasc Res Program, Tucson, AZ 85721 USA Icahn Sch Med Mt Sinai, Dept Med, New York, NY 10029 USA Icahn Sch Med Mt Sinai, Cardiovasc Res Inst, New York, NY 10029 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USANelson, Stanly论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USATouma, Marlin论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Neonatal Congenital Heart Lab, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Los Angeles, CA 90095 USA Univ Calif Los Angeles, Mol Biol Inst, Los Angeles, CA 90095 USA Univ Calif Los Angeles, Eli & Edyth Broad Stem Cell Res Ctr, Los Angeles, CA 90095 USA Univ Calif Los Angeles, Childrens Discovery & Innovat Inst, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Cardiovasc Res Labs, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA
- [36] Whole-Exome Sequencing Identifies a Novel Mutation (p.L320R) of Alpha-Actinin 2 in a Chinese Family with Dilated Cardiomyopathy and Ventricular TachycardiaCYTOGENETIC AND GENOME RESEARCH, 2019, 157 (03) : 148 - 152Fan, Liang-Liang论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Dept Cell Biol, Sch Life Sci, Changsha 410013, Hunan, Peoples R China Cent S Univ, Dept Cell Biol, Sch Life Sci, Changsha 410013, Hunan, Peoples R ChinaHuang, Hao论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Dept Cell Biol, Sch Life Sci, Changsha 410013, Hunan, Peoples R China Cent S Univ, Dept Cell Biol, Sch Life Sci, Changsha 410013, Hunan, Peoples R ChinaJin, Jie-Yuan论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Dept Cell Biol, Sch Life Sci, Changsha 410013, Hunan, Peoples R China Cent S Univ, Dept Cell Biol, Sch Life Sci, Changsha 410013, Hunan, Peoples R ChinaLi, Jing-Jing论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Dept Cell Biol, Sch Life Sci, Changsha 410013, Hunan, Peoples R China Cent S Univ, Dept Cell Biol, Sch Life Sci, Changsha 410013, Hunan, Peoples R ChinaChen, Ya-Qin论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp 2, Dept Cardiol, Changsha, Hunan, Peoples R China Cent S Univ, Dept Cell Biol, Sch Life Sci, Changsha 410013, Hunan, Peoples R ChinaXiang, Rong论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Dept Cell Biol, Sch Life Sci, Changsha 410013, Hunan, Peoples R China Cent S Univ, Xiangya Hosp 2, Dept Cardiol, Changsha, Hunan, Peoples R China Cent S Univ, Dept Cell Biol, Sch Life Sci, Changsha 410013, Hunan, Peoples R China
- [37] Whole-exome sequencing identifies a novel CPT2 mutation in a pedigree with gout (vol 10, 802635, 2022)FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2022, 10Guo, Yong论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, Dept Urol, Affiliated Hosp 1, Wenzhou, Peoples R China Wenzhou Med Univ, Dept Urol, Affiliated Hosp 1, Wenzhou, Peoples R ChinaJin, Jing论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Prov Peoples Hosp, Affiliated Peoples Hosp, Hangzhou Med Coll, Zhejiang Ctr Clin Lab, Hangzhou, Peoples R China Wenzhou Med Univ, Dept Urol, Affiliated Hosp 1, Wenzhou, Peoples R ChinaZhou, Zhenni论文数: 0 引用数: 0 h-index: 0机构: Yueqing Peoples Hosp, Dept Internal Med, Yueqing, Peoples R China Wenzhou Med Univ, Dept Urol, Affiliated Hosp 1, Wenzhou, Peoples R ChinaChen, Yihui论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, Wenzhou, Peoples R China Wenzhou Med Univ, Dept Urol, Affiliated Hosp 1, Wenzhou, Peoples R ChinaSun, Li论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, Dept Rheumatol, Affiliated Hosp 1, Wenzhou, Peoples R China Wenzhou Med Univ, Dept Urol, Affiliated Hosp 1, Wenzhou, Peoples R ChinaZhang, Chunwu论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, Dept Injury Orthopaed, Affiliated Hosp 1, Wenzhou, Peoples R China Wenzhou Med Univ, Dept Urol, Affiliated Hosp 1, Wenzhou, Peoples R ChinaXia, Xiaoru论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, Dept Rheumatol, Affiliated Hosp 1, Wenzhou, Peoples R China Wenzhou Med Univ, Dept Urol, Affiliated Hosp 1, Wenzhou, Peoples R China
- [38] Novel ECHS1 mutations in Leigh syndrome identified by whole-exome sequencing in five Chinese families: case reportBMC MEDICAL GENETICS, 2020, 21 (01)Sun, Dan论文数: 0 引用数: 0 h-index: 0机构: Huazhong Univ Sci & Technol, Wuhan Childrens Hosp, Tongji Med Coll, Dept Pediat Neurol, Wuhan 430016, Peoples R China Huazhong Univ Sci & Technol, Wuhan Childrens Hosp, Tongji Med Coll, Dept Pediat Neurol, Wuhan 430016, Peoples R ChinaLiu, Zhimei论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing 100045, Peoples R China Huazhong Univ Sci & Technol, Wuhan Childrens Hosp, Tongji Med Coll, Dept Pediat Neurol, Wuhan 430016, Peoples R ChinaLiu, Yongchu论文数: 0 引用数: 0 h-index: 0机构: Aegicare Shenzhen Technol Co Ltd, Shenzhen 518110, Peoples R China Huazhong Univ Sci & Technol, Wuhan Childrens Hosp, Tongji Med Coll, Dept Pediat Neurol, Wuhan 430016, Peoples R ChinaWu, Miaojuan论文数: 0 引用数: 0 h-index: 0机构: Jianghan Univ, Sch Med, Wuhan 430056, Peoples R China Huazhong Univ Sci & Technol, Wuhan Childrens Hosp, Tongji Med Coll, Dept Pediat Neurol, Wuhan 430016, Peoples R ChinaFang, Fang论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Neurol, Beijing 100045, Peoples R China Huazhong Univ Sci & Technol, Wuhan Childrens Hosp, Tongji Med Coll, Dept Pediat Neurol, Wuhan 430016, Peoples R ChinaDeng, Xianbo论文数: 0 引用数: 0 h-index: 0机构: Huazhong Univ Sci & Technol, Union Hosp, Radiol Dept, Wuhan 430056, Peoples R China Huazhong Univ Sci & Technol, Wuhan Childrens Hosp, Tongji Med Coll, Dept Pediat Neurol, Wuhan 430016, Peoples R ChinaLiu, Zhisheng论文数: 0 引用数: 0 h-index: 0机构: Huazhong Univ Sci & Technol, Wuhan Childrens Hosp, Tongji Med Coll, Dept Pediat Neurol, Wuhan 430016, Peoples R China Huazhong Univ Sci & Technol, Wuhan Childrens Hosp, Tongji Med Coll, Dept Pediat Neurol, Wuhan 430016, Peoples R ChinaSong, Liang论文数: 0 引用数: 0 h-index: 0机构: Third Peoples Hosp Hubei Prov, Wuhan 430030, Peoples R China Huazhong Univ Sci & Technol, Wuhan Childrens Hosp, Tongji Med Coll, Dept Pediat Neurol, Wuhan 430016, Peoples R ChinaMurayama, Kei论文数: 0 引用数: 0 h-index: 0机构: Chiba Childrens Hosp, Ctr Med Genet, Dept Metab, Chiba 2660007, Japan Huazhong Univ Sci & Technol, Wuhan Childrens Hosp, Tongji Med Coll, Dept Pediat Neurol, Wuhan 430016, Peoples R ChinaZhang, Chunhua论文数: 0 引用数: 0 h-index: 0机构: MILS Int, Yokohama, Kanagawa 2220033, Japan Huazhong Univ Sci & Technol, Wuhan Childrens Hosp, Tongji Med Coll, Dept Pediat Neurol, Wuhan 430016, Peoples R ChinaZhu, Yuanyuan论文数: 0 引用数: 0 h-index: 0机构: Aegicare Shenzhen Technol Co Ltd, Shenzhen 518110, Peoples R China Huazhong Univ Sci & Technol, Wuhan Childrens Hosp, Tongji Med Coll, Dept Pediat Neurol, Wuhan 430016, Peoples R China
- [39] Whole-Exome Sequencing Analysis Identified Novel Mutations in the TSPAN12 Gene in Chinese Families with Familial Exudative VitreoretinopathyGENETIC TESTING AND MOLECULAR BIOMARKERS, 2019, 23 (10) : 722 - 727Yuan, Ye论文数: 0 引用数: 0 h-index: 0机构: Chengdu Univ Tradit Chinese Med, Coll Med Technol, 37 Twelve Bridge Rd, Chengdu 610075, Sichuan, Peoples R China Chengdu Univ Tradit Chinese Med, Coll Med Technol, 37 Twelve Bridge Rd, Chengdu 610075, Sichuan, Peoples R ChinaXu, Huijuan论文数: 0 引用数: 0 h-index: 0机构: Univ Elect Sci & Technol China, Sichuan Acad Med Sci, Key Lab Human Dis Gene Study, First Ring Rd,West 2, Chengdu 610072, Sichuan, Peoples R China Univ Elect Sci & Technol China, Sichuan Peoples Hosp, Sch Med, First Ring Rd,West 2, Chengdu 610072, Sichuan, Peoples R China Chinese Acad Sci, Chengdu Inst Biol, Chengdu, Sichuan, Peoples R China Chengdu Univ Tradit Chinese Med, Coll Med Technol, 37 Twelve Bridge Rd, Chengdu 610075, Sichuan, Peoples R ChinaZhang, Shanshan论文数: 0 引用数: 0 h-index: 0机构: Univ Elect Sci & Technol China, Sichuan Acad Med Sci, Key Lab Human Dis Gene Study, First Ring Rd,West 2, Chengdu 610072, Sichuan, Peoples R China Univ Elect Sci & Technol China, Sichuan Peoples Hosp, Sch Med, First Ring Rd,West 2, Chengdu 610072, Sichuan, Peoples R China Chengdu Univ Tradit Chinese Med, Coll Med Technol, 37 Twelve Bridge Rd, Chengdu 610075, Sichuan, Peoples R ChinaZhang, Xiang论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Sch Med, Xinhua Hosp, Dept Ophthalmol, Shanghai, Peoples R China Chengdu Univ Tradit Chinese Med, Coll Med Technol, 37 Twelve Bridge Rd, Chengdu 610075, Sichuan, Peoples R ChinaZhang, Lin论文数: 0 引用数: 0 h-index: 0机构: Univ Elect Sci & Technol China, Sichuan Acad Med Sci, Key Lab Human Dis Gene Study, First Ring Rd,West 2, Chengdu 610072, Sichuan, Peoples R China Univ Elect Sci & Technol China, Sichuan Peoples Hosp, Sch Med, First Ring Rd,West 2, Chengdu 610072, Sichuan, Peoples R China Chengdu Univ Tradit Chinese Med, Coll Med Technol, 37 Twelve Bridge Rd, Chengdu 610075, Sichuan, Peoples R ChinaYang, Zhenglin论文数: 0 引用数: 0 h-index: 0机构: Chengdu Univ Tradit Chinese Med, Coll Med Technol, 37 Twelve Bridge Rd, Chengdu 610075, Sichuan, Peoples R China Univ Elect Sci & Technol China, Sichuan Acad Med Sci, Key Lab Human Dis Gene Study, First Ring Rd,West 2, Chengdu 610072, Sichuan, Peoples R China Univ Elect Sci & Technol China, Sichuan Peoples Hosp, Sch Med, First Ring Rd,West 2, Chengdu 610072, Sichuan, Peoples R China Chinese Acad Sci, Chengdu Inst Biol, Chengdu, Sichuan, Peoples R China Chengdu Univ Tradit Chinese Med, Coll Med Technol, 37 Twelve Bridge Rd, Chengdu 610075, Sichuan, Peoples R China
- [40] Whole-Exome Sequencing Identifies Novel Somatic Mutations Associated with Prognosis in Lung Cancer Metastatic to the BrainJOURNAL OF THORACIC ONCOLOGY, 2019, 14 (10) : S373 - S374Su, C.论文数: 0 引用数: 0 h-index: 0机构: Shanghai Pulm Hosp, Shanghai, Peoples R China Shanghai Pulm Hosp, Shanghai, Peoples R ChinaLi, X.论文数: 0 引用数: 0 h-index: 0机构: Shanghai Pulm Hosp, Shanghai, Peoples R China Shanghai Pulm Hosp, Shanghai, Peoples R ChinaZhao, C.论文数: 0 引用数: 0 h-index: 0机构: Shanghai Pulm Hosp, Shanghai, Peoples R China Shanghai Pulm Hosp, Shanghai, Peoples R ChinaZhao, J.论文数: 0 引用数: 0 h-index: 0机构: Shanghai Pulm Hosp, Shanghai, Peoples R China Shanghai Pulm Hosp, Shanghai, Peoples R China