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- [1] DNA Sequence Capture and High Throughput Sequencing Technology: a Novel Approach to Identify a Large Number of Hypertrophic Cardiomyopathy-causing GenesCIRCULATION, 2010, 122 (21)D'Argenio, Valeria论文数: 0 引用数: 0 h-index: 0机构: CEINGE Biotecnol Avanzate, Naples, ItalyFrisso, Giulia论文数: 0 引用数: 0 h-index: 0机构: CEINGE Biotecnol Avanzate, Naples, ItalyLimongelli, Giuseppe论文数: 0 引用数: 0 h-index: 0机构: CEINGE Biotecnol Avanzate, Naples, ItalyPrecone, Vincenza论文数: 0 引用数: 0 h-index: 0机构: CEINGE Biotecnol Avanzate, Naples, ItalyPacileo, Giuseppe论文数: 0 引用数: 0 h-index: 0机构: CEINGE Biotecnol Avanzate, Naples, ItalyFienga, Antonella论文数: 0 引用数: 0 h-index: 0机构: CEINGE Biotecnol Avanzate, Naples, ItalyBoccia, Angelo论文数: 0 引用数: 0 h-index: 0机构: CEINGE Biotecnol Avanzate, Naples, ItalyCalabro, Raffaele论文数: 0 引用数: 0 h-index: 0机构: CEINGE Biotecnol Avanzate, Naples, ItalyPaolella, Giovanni论文数: 0 引用数: 0 h-index: 0机构: CEINGE Biotecnol Avanzate, Naples, ItalySalvatore, Francesco论文数: 0 引用数: 0 h-index: 0机构: CEINGE Biotecnol Avanzate, Naples, Italy
- [2] Identification of Sequence Variants in Genetic Disease-Causing Genes Using Targeted Next-Generation SequencingPLOS ONE, 2011, 6 (12):Wei, Xiaoming论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R ChinaJu, Xiangchun论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R ChinaYi, Xin论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R ChinaZhu, Qian论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R ChinaQu, Ning论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R ChinaLiu, Tengfei论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R ChinaChen, Yang论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R ChinaJiang, Hui论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R ChinaYang, Guanghui论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R ChinaZhen, Ruan论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R ChinaLan, Zhangzhang论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R ChinaQi, Ming论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R ChinaWang, Jinming论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R ChinaYang, Yi论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R ChinaChu, Yuxing论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R ChinaLi, Xiaoyan论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R ChinaGuang, Yanfang论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R ChinaHuang, Jian论文数: 0 引用数: 0 h-index: 0机构: Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China Natl Engn Ctr Biochip Shanghai, Shanghai Minist Key Lab Dis & Hlth Genom, Shanghai, Peoples R China Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China
- [3] Application of Whole-Exome and Retinal-Capture Next-Generation DNA Sequencing to Identify Disease-Causing Mutations in Families with a Diagnosis of Autosomal Dominant Retinitis PigmentosaINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2013, 54 (15)Daiger, Stephen论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Hlth Sci Ctr Houston, Ctr Human Genet, Sch Publ Hlth, Houston, TX 77030 USA Univ Texas Hlth Sci Ctr Houston, Ctr Human Genet, Sch Publ Hlth, Houston, TX 77030 USASullivan, Lori论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Hlth Sci Ctr Houston, Ctr Human Genet, Sch Publ Hlth, Houston, TX 77030 USA Univ Texas Hlth Sci Ctr Houston, Ctr Human Genet, Sch Publ Hlth, Houston, TX 77030 USABowne, Sara论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Hlth Sci Ctr Houston, Ctr Human Genet, Sch Publ Hlth, Houston, TX 77030 USA Univ Texas Hlth Sci Ctr Houston, Ctr Human Genet, Sch Publ Hlth, Houston, TX 77030 USAWeinstock, George论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Genome Inst, St Louis, MO USA Univ Texas Hlth Sci Ctr Houston, Ctr Human Genet, Sch Publ Hlth, Houston, TX 77030 USAKoboldt, Daniel论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Genome Inst, St Louis, MO USA Univ Texas Hlth Sci Ctr Houston, Ctr Human Genet, Sch Publ Hlth, Houston, TX 77030 USAChen, Rui论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Univ Texas Hlth Sci Ctr Houston, Ctr Human Genet, Sch Publ Hlth, Houston, TX 77030 USAHeckenlively, John论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Kellogg Eye Ctr, Ann Arbor, MI 48109 USA Univ Texas Hlth Sci Ctr Houston, Ctr Human Genet, Sch Publ Hlth, Houston, TX 77030 USABranham, Kari论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Kellogg Eye Ctr, Ann Arbor, MI 48109 USA Univ Texas Hlth Sci Ctr Houston, Ctr Human Genet, Sch Publ Hlth, Houston, TX 77030 USABirch, David论文数: 0 引用数: 0 h-index: 0机构: Retina Fdn Southwest, Dallas, TX USA Univ Texas Hlth Sci Ctr Houston, Ctr Human Genet, Sch Publ Hlth, Houston, TX 77030 USAWheaton, Dianna论文数: 0 引用数: 0 h-index: 0机构: Retina Fdn Southwest, Dallas, TX USA Univ Texas Hlth Sci Ctr Houston, Ctr Human Genet, Sch Publ Hlth, Houston, TX 77030 USA
- [4] The Use of Capture Array and Next Generation Sequencing for Genes in the Ras PathwayJOURNAL OF MOLECULAR DIAGNOSTICS, 2010, 12 (06): : 863 - 863Zborovski, T. M. Muram论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Salt Lake City, UT USA ARUP Labs, Salt Lake City, UT USA Univ Utah, Salt Lake City, UT USAStevenson, D. A.论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Salt Lake City, UT USA Univ Utah, Salt Lake City, UT USAViskochil, D. H.论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Salt Lake City, UT USA Univ Utah, Salt Lake City, UT USAMao, R.论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Salt Lake City, UT USA ARUP Labs, Salt Lake City, UT USA Univ Utah, Salt Lake City, UT USA
- [5] Sequence Capture And Next Generation Sequencing In Paediatric DNA Repair DisordersJOURNAL OF MEDICAL GENETICS, 2012, 49 : S117 - S117Sutton, Ruth论文数: 0 引用数: 0 h-index: 0Gabriel, J.论文数: 0 引用数: 0 h-index: 0Wilson, B. T.论文数: 0 引用数: 0 h-index: 0
- [6] Next Generation Sequencing (NGS) panel revealed new candidate genes and variants in 25 Hypertrophic Cardiomyopathy patientsEUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 150 - 150Turkgenc, B.论文数: 0 引用数: 0 h-index: 0机构: Acibadem Genet Diagnost Ctr, Istanbul, Turkey Acibadem Genet Diagnost Ctr, Istanbul, TurkeyTemel, S. G.论文数: 0 引用数: 0 h-index: 0机构: Uludag Univ, Fac Med, Dept Med Genet, Bursa, Turkey Uludag Univ, Fac Med, Dept Histol & Embryol, Bursa, Turkey Acibadem Genet Diagnost Ctr, Istanbul, TurkeyUysal, F.论文数: 0 引用数: 0 h-index: 0机构: Uludag Univ, Fac Med, Dept Pediat Cardiol, Bursa, Turkey Acibadem Genet Diagnost Ctr, Istanbul, TurkeyAtik, S. Ugan论文数: 0 引用数: 0 h-index: 0机构: Cerrahpasa Med Fac, Dept Pediat Cardiol, Istanbul, Turkey Acibadem Genet Diagnost Ctr, Istanbul, TurkeyOztunc, F.论文数: 0 引用数: 0 h-index: 0机构: Cerrahpasa Med Fac, Dept Pediat Cardiol, Istanbul, Turkey Acibadem Genet Diagnost Ctr, Istanbul, TurkeySulu, A.论文数: 0 引用数: 0 h-index: 0机构: Gaziantep Univ, Fac Med, Dept Pediat Cardiol, Gaziantep, Turkey Acibadem Genet Diagnost Ctr, Istanbul, TurkeyEkici, F.论文数: 0 引用数: 0 h-index: 0机构: Akdeniz Univ, Fac Med, Dept Pediat Cardiol, Antalya, Turkey Acibadem Genet Diagnost Ctr, Istanbul, TurkeyAyabakan, C.论文数: 0 引用数: 0 h-index: 0机构: Baskent Univ, Istanbul Hosp, Dept Pediat Cardiol, Istanbul, Turkey Acibadem Genet Diagnost Ctr, Istanbul, TurkeyOdemis, E.论文数: 0 引用数: 0 h-index: 0机构: Acibadem Univ, Acibadem Atakent Hosp, Dept Pediat Cardiol, Istanbul, Turkey Acibadem Genet Diagnost Ctr, Istanbul, TurkeySaygili, A.论文数: 0 引用数: 0 h-index: 0机构: Acibadem Univ, Fac Med, Dept Pediat Cardiol, Istanbul, Turkey Acibadem Genet Diagnost Ctr, Istanbul, TurkeyKoka, A.论文数: 0 引用数: 0 h-index: 0机构: Cerrahpasa Med Fac, Dept Pediat Cardiol, Istanbul, Turkey Acibadem Genet Diagnost Ctr, Istanbul, TurkeyAkinci, I. Ozkan论文数: 0 引用数: 0 h-index: 0机构: Istanbul Med Fac, Dept Anesthesiol & Reanimat, Istanbul, Turkey Acibadem Genet Diagnost Ctr, Istanbul, TurkeyAlanay, Y.论文数: 0 引用数: 0 h-index: 0机构: Acibadem Univ, Dept Med Genet, Istanbul, Turkey Acibadem Maslak Hosp, Dept Pediat Genet, Istanbul, Turkey Acibadem Genet Diagnost Ctr, Istanbul, TurkeyCeliker, A.论文数: 0 引用数: 0 h-index: 0机构: Koc Univ, Fac Med, Dept Pediat Cardiol, Istanbul, Turkey Acibadem Genet Diagnost Ctr, Istanbul, TurkeyOzer, A.论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Dept Med Biol & Genet, Istanbul, Turkey Acibadem Genet Diagnost Ctr, Istanbul, TurkeyYakicier, M. C.论文数: 0 引用数: 0 h-index: 0机构: Acibadem Univ, Fac Sci, Dept Mol Biol & Genet, Istanbul, Turkey Acibadem Genet Diagnost Ctr, Istanbul, Turkey
- [7] Identification of Disease-Causing Mutations in Autosomal Dominant Retinitis Pigmentosa (adRP) Using Next-Generation DNA SequencingINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2011, 52 (01) : 494 - 503Bowne, Sara J.论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USA Univ Texas Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USASullivan, Lori S.论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USA Univ Texas Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USAKoboldt, Daniel C.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Genome Sequencing Ctr, St Louis, MO USA Univ Texas Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USADing, Li论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Genome Sequencing Ctr, St Louis, MO USA Univ Texas Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USAFulton, Robert论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Genome Sequencing Ctr, St Louis, MO USA Univ Texas Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USAAbbott, Rachel M.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Genome Sequencing Ctr, St Louis, MO USA Univ Texas Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USASodergren, Erica J.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Genome Sequencing Ctr, St Louis, MO USA Univ Texas Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USABirch, David G.论文数: 0 引用数: 0 h-index: 0机构: Retina Fdn SW, Dallas, TX USA Univ Texas Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USAWheaton, Dianna H.论文数: 0 引用数: 0 h-index: 0机构: Retina Fdn SW, Dallas, TX USA Univ Texas Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USAHeckenlively, John R.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Kellogg Eye Ctr, Ann Arbor, MI 48109 USA Univ Texas Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USALiu, Qin论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Sch Med, FM Kirby Ctr Mol Ophthalmol, Philadelphia, PA 19104 USA Univ Texas Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USAPierce, Eric A.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Sch Med, FM Kirby Ctr Mol Ophthalmol, Philadelphia, PA 19104 USA Univ Texas Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USAWeinstock, George M.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Genome Sequencing Ctr, St Louis, MO USA Univ Texas Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USADaiger, Stephen P.论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USA Univ Texas Hlth Sci Ctr, Ctr Human Genet, Houston, TX 77030 USA
- [8] Using next-generation sequencing to identify novel disease genesBRITISH JOURNAL OF DERMATOLOGY, 2011, 164 (04) : 930 - 931Blaydon, D. C.论文数: 0 引用数: 0 h-index: 0机构: Univ London, Barts & London Sch Med & Dent, Blizard Inst Cell & Mol Sci, London, England Univ London, Barts & London Sch Med & Dent, Blizard Inst Cell & Mol Sci, London, EnglandWalne, A. J.论文数: 0 引用数: 0 h-index: 0机构: Univ London, Barts & London Sch Med & Dent, Blizard Inst Cell & Mol Sci, London, England Univ London, Barts & London Sch Med & Dent, Blizard Inst Cell & Mol Sci, London, EnglandPlagnol, V.论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Addenbrookes Hosp, Wellcome Trust Diabet & Inflammat Lab, Juvenile Diabet Res Fdn,Cambridge Inst Med Res, Cambridge CB2 2QQ, England Univ London, Barts & London Sch Med & Dent, Blizard Inst Cell & Mol Sci, London, Englandvan Heel, D. A.论文数: 0 引用数: 0 h-index: 0机构: Univ London, Barts & London Sch Med & Dent, Blizard Inst Cell & Mol Sci, London, England Univ London, Barts & London Sch Med & Dent, Blizard Inst Cell & Mol Sci, London, EnglandVulliamy, T.论文数: 0 引用数: 0 h-index: 0机构: Univ London, Barts & London Sch Med & Dent, Blizard Inst Cell & Mol Sci, London, England Univ London, Barts & London Sch Med & Dent, Blizard Inst Cell & Mol Sci, London, EnglandKelsell, D. P.论文数: 0 引用数: 0 h-index: 0机构: Univ London, Barts & London Sch Med & Dent, Blizard Inst Cell & Mol Sci, London, England Univ London, Barts & London Sch Med & Dent, Blizard Inst Cell & Mol Sci, London, England
- [9] Applying next generation sequencing with microdroplet PCR to determine the disease-causing mutations in retinal dystrophiesBMC Ophthalmology, 17Xinjing Wang论文数: 0 引用数: 0 h-index: 0机构: Ophthalmic Genetics and Visual Function Branch,Wadih M. Zein论文数: 0 引用数: 0 h-index: 0机构: Ophthalmic Genetics and Visual Function Branch,Leera D’Souza论文数: 0 引用数: 0 h-index: 0机构: Ophthalmic Genetics and Visual Function Branch,Chimere Roberson论文数: 0 引用数: 0 h-index: 0机构: Ophthalmic Genetics and Visual Function Branch,Keith Wetherby论文数: 0 引用数: 0 h-index: 0机构: Ophthalmic Genetics and Visual Function Branch,Hong He论文数: 0 引用数: 0 h-index: 0机构: Ophthalmic Genetics and Visual Function Branch,Angela Villarta论文数: 0 引用数: 0 h-index: 0机构: Ophthalmic Genetics and Visual Function Branch,Amy Turriff论文数: 0 引用数: 0 h-index: 0机构: Ophthalmic Genetics and Visual Function Branch,Kory R. Johnson论文数: 0 引用数: 0 h-index: 0机构: Ophthalmic Genetics and Visual Function Branch,Yang C. Fann论文数: 0 引用数: 0 h-index: 0机构: Ophthalmic Genetics and Visual Function Branch,
- [10] Applying next generation sequencing with microdroplet PCR to determine the disease-causing mutations in retinal dystrophiesBMC OPHTHALMOLOGY, 2017, 17Wang, Xinjing论文数: 0 引用数: 0 h-index: 0机构: NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USA NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USAZein, Wadih M.论文数: 0 引用数: 0 h-index: 0机构: NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USA NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USAD'Souza, Leera论文数: 0 引用数: 0 h-index: 0机构: NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USA NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USARoberson, Chimere论文数: 0 引用数: 0 h-index: 0机构: NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USA NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USAWetherby, Keith论文数: 0 引用数: 0 h-index: 0机构: NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USA NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USAHe, Hong论文数: 0 引用数: 0 h-index: 0机构: NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USA NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USAVillarta, Angela论文数: 0 引用数: 0 h-index: 0机构: NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USA NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USATurriff, Amy论文数: 0 引用数: 0 h-index: 0机构: NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USA NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USAJohnson, Kory R.论文数: 0 引用数: 0 h-index: 0机构: NINDS, Intramural IT & Bioinformat Program, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USAFann, Yang C.论文数: 0 引用数: 0 h-index: 0机构: NINDS, Intramural IT & Bioinformat Program, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA NEI, Ophthalm Genet & Visual Funct Branch, NIH, 10D43,10 Ctr Dr, Bethesda, MD 20892 USA