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- [1] Genetic heterogeneity of Usher syndrome: Analysis of 151 families with Usher type IAMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (06) : 1569 - 1574Astuto, LM论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USAWeston, MD论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USACarney, CA论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USAHoover, DM论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USACremers, CWRJ论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USAWagenaar, M论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USAMoller, C论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USASmith, RJH论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USAPieke-Dahl, S论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USAGreenberg, J论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USARamesar, R论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USAJacobson, SG论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USAAyuso, C论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USAHeckenlively, JR论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USATamayo, M论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USAGorin, MB论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USAReardon, W论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USAKimerling, WJ论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Ctr Hereditary Commun Disorders, Omaha, NE 68131 USA
- [2] Comprehensive Molecular Screening in a Large Chinese Cohort with Usher SyndromeINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2018, 59 (09)Sun, Tengyang论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Beijing, Peoples R China Capital Med Univ, Beijing, Peoples R ChinaXu, Ke论文数: 0 引用数: 0 h-index: 0机构: Beijing Inst Ophthalmol, Beijing, Peoples R China Capital Med Univ, Beijing, Peoples R ChinaZhang, Xiaohui论文数: 0 引用数: 0 h-index: 0机构: Beijing Inst Ophthalmol, Beijing, Peoples R China Capital Med Univ, Beijing, Peoples R ChinaLi, Yang论文数: 0 引用数: 0 h-index: 0机构: Beijing Inst Ophthalmol, Beijing, Peoples R China Capital Med Univ, Beijing, Peoples R China
- [3] Phenotypic and Genetic Characteristics in a Cohort of Patients with Usher GenesGENES, 2022, 13 (08)Feenstra, Helena M.论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Nuffield Dept Clin Neurosci, Nuffield Lab Ophthalmol, Oxford OX3 9DU, England Univ Oxford, Nuffield Dept Clin Neurosci, Nuffield Lab Ophthalmol, Oxford OX3 9DU, EnglandAl-Khuzaei, Saoud论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Nuffield Dept Clin Neurosci, Nuffield Lab Ophthalmol, Oxford OX3 9DU, England Oxford Univ Hosp NHS Fdn Trust, Oxford Eye Hosp, Oxford OX3 9DU, England Univ Oxford, Nuffield Dept Clin Neurosci, Nuffield Lab Ophthalmol, Oxford OX3 9DU, England论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Shanks, Morag论文数: 0 引用数: 0 h-index: 0机构: Oxford Univ Hosp NHS Fdn Trust, Oxford Med Genet Labs, Oxford OX3 7LE, England Univ Oxford, Nuffield Dept Clin Neurosci, Nuffield Lab Ophthalmol, Oxford OX3 9DU, EnglandKamath, Archith论文数: 0 引用数: 0 h-index: 0机构: Oxford Univ Hosp NHS Fdn Trust, Oxford Eye Hosp, Oxford OX3 9DU, England Univ Oxford, Nuffield Dept Clin Neurosci, Nuffield Lab Ophthalmol, Oxford OX3 9DU, EnglandYu, Jing论文数: 0 引用数: 0 h-index: 0机构: Oxford Univ Hosp NHS Fdn Trust, Oxford Eye Hosp, Oxford OX3 9DU, England Univ Oxford, Wellcome Ctr Human Genet, NIHR Oxford Biomed Res Ctr, Oxford OX3 7BN, England Univ Oxford, Nuffield Dept Clin Neurosci, Nuffield Lab Ophthalmol, Oxford OX3 9DU, EnglandJolly, Jasleen K.论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Nuffield Dept Clin Neurosci, Nuffield Lab Ophthalmol, Oxford OX3 9DU, England Oxford Univ Hosp NHS Fdn Trust, Oxford Eye Hosp, Oxford OX3 9DU, England Anglia Ruskin Univ, Vis & Eye Res Inst, Cambridge CB1 1PT, England Univ Oxford, Nuffield Dept Clin Neurosci, Nuffield Lab Ophthalmol, Oxford OX3 9DU, EnglandMacLaren, Robert E.论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Nuffield Dept Clin Neurosci, Nuffield Lab Ophthalmol, Oxford OX3 9DU, England Oxford Univ Hosp NHS Fdn Trust, Oxford Eye Hosp, Oxford OX3 9DU, England Univ Oxford, Nuffield Dept Clin Neurosci, Nuffield Lab Ophthalmol, Oxford OX3 9DU, EnglandClouston, Penny论文数: 0 引用数: 0 h-index: 0机构: Oxford Univ Hosp NHS Fdn Trust, Oxford Med Genet Labs, Oxford OX3 7LE, England Univ Oxford, Nuffield Dept Clin Neurosci, Nuffield Lab Ophthalmol, Oxford OX3 9DU, EnglandHalford, Stephanie论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Nuffield Dept Clin Neurosci, Nuffield Lab Ophthalmol, Oxford OX3 9DU, England Univ Oxford, Nuffield Dept Clin Neurosci, Nuffield Lab Ophthalmol, Oxford OX3 9DU, EnglandDownes, Susan M.论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Nuffield Dept Clin Neurosci, Nuffield Lab Ophthalmol, Oxford OX3 9DU, England Oxford Univ Hosp NHS Fdn Trust, Oxford Eye Hosp, Oxford OX3 9DU, England Univ Oxford, Nuffield Dept Clin Neurosci, Nuffield Lab Ophthalmol, Oxford OX3 9DU, England
- [4] Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient populationHUMAN GENETICS, 2005, 116 (04) : 292 - 299Ouyang, XM论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Otolaryngol, Miami, FL 33136 USAYan, D论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Otolaryngol, Miami, FL 33136 USADu, LL论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Otolaryngol, Miami, FL 33136 USAHejtmancik, JF论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Otolaryngol, Miami, FL 33136 USAJacobson, SG论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Otolaryngol, Miami, FL 33136 USANance, WE论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Otolaryngol, Miami, FL 33136 USALi, AR论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Otolaryngol, Miami, FL 33136 USAAngeli, S论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Otolaryngol, Miami, FL 33136 USAKaiser, M论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Otolaryngol, Miami, FL 33136 USANewton, V论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Otolaryngol, Miami, FL 33136 USABrown, SDM论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Otolaryngol, Miami, FL 33136 USABalkany, T论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Otolaryngol, Miami, FL 33136 USALiu, XZ论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Otolaryngol, Miami, FL 33136 USA
- [5] Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient populationHuman Genetics, 2005, 116 : 292 - 299Xiao Mei Ouyang论文数: 0 引用数: 0 h-index: 0机构: University of Miami,Department of Otolaryngology (DDenise Yan论文数: 0 引用数: 0 h-index: 0机构: University of Miami,Department of Otolaryngology (DLi Lin Du论文数: 0 引用数: 0 h-index: 0机构: University of Miami,Department of Otolaryngology (DJ. Fielding. Hejtmancik论文数: 0 引用数: 0 h-index: 0机构: University of Miami,Department of Otolaryngology (DSamuel G. Jacobson论文数: 0 引用数: 0 h-index: 0机构: University of Miami,Department of Otolaryngology (DWalter E. Nance论文数: 0 引用数: 0 h-index: 0机构: University of Miami,Department of Otolaryngology (DAn Ren Li论文数: 0 引用数: 0 h-index: 0机构: University of Miami,Department of Otolaryngology (DSimon Angeli论文数: 0 引用数: 0 h-index: 0机构: University of Miami,Department of Otolaryngology (DMuriel Kaiser论文数: 0 引用数: 0 h-index: 0机构: University of Miami,Department of Otolaryngology (DValerie Newton论文数: 0 引用数: 0 h-index: 0机构: University of Miami,Department of Otolaryngology (DSteve D. M. Brown论文数: 0 引用数: 0 h-index: 0机构: University of Miami,Department of Otolaryngology (DThomas Balkany论文数: 0 引用数: 0 h-index: 0机构: University of Miami,Department of Otolaryngology (DXue Zhong Liu论文数: 0 引用数: 0 h-index: 0机构: University of Miami,Department of Otolaryngology (D
- [6] Comprehensive Genetic Analysis of a Hungarian Amyotrophic Lateral Sclerosis CohortFRONTIERS IN GENETICS, 2019, 10Tripolszki, Kornelia论文数: 0 引用数: 0 h-index: 0机构: Univ Szeged, Dept Med Genet, Szeged, Hungary Univ Szeged, Dept Med Genet, Szeged, Hungary论文数: 引用数: h-index:机构:Schmidt, Helena论文数: 0 引用数: 0 h-index: 0机构: Med Univ Graz, Res Unit Genet Epidemiol, Gottfried Schatz Res Ctr, Mol Biol & Biochem, Graz, Austria Univ Szeged, Dept Med Genet, Szeged, HungaryNagy, Zsofia F.论文数: 0 引用数: 0 h-index: 0机构: Univ Szeged, Dept Med Genet, Szeged, Hungary Univ Szeged, Dept Med Genet, Szeged, HungaryNagy, Dora论文数: 0 引用数: 0 h-index: 0机构: Univ Szeged, Dept Med Genet, Szeged, Hungary Univ Szeged, Dept Med Genet, Szeged, HungaryKlivenyi, Peter论文数: 0 引用数: 0 h-index: 0机构: Univ Szeged, Dept Neurol, Szeged, Hungary Univ Szeged, Dept Med Genet, Szeged, HungaryEngelhardt, Jozsef, I论文数: 0 引用数: 0 h-index: 0机构: Univ Szeged, Dept Neurol, Szeged, Hungary Univ Szeged, Dept Med Genet, Szeged, HungarySzell, Marta论文数: 0 引用数: 0 h-index: 0机构: Univ Szeged, Dept Med Genet, Szeged, Hungary Univ Szeged, Dept Med Genet, Szeged, Hungary
- [7] Comprehensive genetic analysis of an italian amyotrophic lateral sclerosis cohortEUROPEAN JOURNAL OF NEUROLOGY, 2020, 27 : 617 - 617Stella, A. Bartoletti论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Sci Neurol Bologna, Bologna, Italy IRCCS Ist Sci Neurol Bologna, Bologna, ItalyVacchiano, V.论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Sci Neurol Bologna, Bologna, Italy IRCCS Ist Sci Neurol Bologna, Bologna, ItalyDe Pasqua, S.论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Sci Neurol Bologna, Bologna, Italy IRCCS Ist Sci Neurol Bologna, Bologna, ItalyBartolomei, I.论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Sci Neurol Bologna, Bologna, Italy IRCCS Ist Sci Neurol Bologna, Bologna, ItalyPastorelli, F.论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Sci Neurol Bologna, Bologna, Italy IRCCS Ist Sci Neurol Bologna, Bologna, ItalyPiras, S.论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Sci Neurol Bologna, Bologna, Italy IRCCS Ist Sci Neurol Bologna, Bologna, ItalyMengozzi, G.论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Sci Neurol Bologna, Bologna, Italy IRCCS Ist Sci Neurol Bologna, Bologna, ItalySalvi, F.论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Sci Neurol Bologna, Bologna, Italy IRCCS Ist Sci Neurol Bologna, Bologna, ItalyParchi, P.论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Sci Neurol Bologna, Bologna, Italy IRCCS Ist Sci Neurol Bologna, Bologna, ItalyLiguori, R.论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Sci Neurol Bologna, Bologna, Italy IRCCS Ist Sci Neurol Bologna, Bologna, ItalyCapellari, S.论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Sci Neurol Bologna, Bologna, Italy IRCCS Ist Sci Neurol Bologna, Bologna, Italy
- [8] Comprehensive sequence analysis of nine Usher syndrome genes in the UK National Collaborative Usher StudyJOURNAL OF MEDICAL GENETICS, 2012, 49 (01) : 27 - 36Stabej, Polona Le Quesne论文数: 0 引用数: 0 h-index: 0机构: UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, EnglandSaihan, Zubin论文数: 0 引用数: 0 h-index: 0机构: UCL, Inst Ophthalmol, London WC1N 1EH, England Moorfields Eye Hosp, London, England UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, EnglandRangesh, Nell论文数: 0 引用数: 0 h-index: 0机构: UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, EnglandSteele-Stallard, Heather B.论文数: 0 引用数: 0 h-index: 0机构: UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, EnglandAmbrose, John论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Inst, Cambridge, England UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, EnglandCoffey, Alison论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Inst, Cambridge, England UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, EnglandEmmerson, Jenny论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Inst, Cambridge, England UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, EnglandHaralambous, Elene论文数: 0 引用数: 0 h-index: 0机构: UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, EnglandHughes, Yasmin论文数: 0 引用数: 0 h-index: 0机构: UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, EnglandSteel, Karen P.论文数: 0 引用数: 0 h-index: 0机构: Wellcome Trust Sanger Inst, Cambridge, England UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, EnglandLuxon, Linda M.论文数: 0 引用数: 0 h-index: 0机构: UCL Ear Inst, London, England UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, EnglandWebster, Andrew R.论文数: 0 引用数: 0 h-index: 0机构: UCL, Inst Ophthalmol, London WC1N 1EH, England Moorfields Eye Hosp, London, England UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, EnglandBitner-Glindzicz, Maria论文数: 0 引用数: 0 h-index: 0机构: UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England UCL, Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
- [9] Genetic landscape and ocular biometric correlations in microspherophakia: insights from a comprehensive patient cohortHUMAN GENOMICS, 2025, 19 (01)Liu, Yan论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Eye & ENT Hosp, Eye Inst, Shanghai 200031, Peoples R China Fudan Univ, Eye & ENT Hosp, Dept Ophthalmol, Shanghai 200031, Peoples R China Chinese Acad Med Sci, Key Lab Myopia Key Lab Myopia & Related Eye Dis, NHC, Shanghai 200031, Peoples R China Chinese Acad Med Sci, Key Lab Myopia & Related Eye Dis, Shanghai 200031, Peoples R China Shanghai Key Lab Visual Impairment & Restorat, Shanghai 200031, Peoples R China Fudan Univ, Eye & ENT Hosp, Eye Inst, Shanghai 200031, Peoples R ChinaSun, Yang论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Eye & ENT Hosp, Eye Inst, Shanghai 200031, Peoples R China Fudan Univ, Eye & ENT Hosp, Dept Ophthalmol, Shanghai 200031, Peoples R China Chinese Acad Med Sci, Key Lab Myopia Key Lab Myopia & Related Eye Dis, NHC, Shanghai 200031, Peoples R China Chinese Acad Med Sci, Key Lab Myopia & Related Eye Dis, Shanghai 200031, Peoples R China Shanghai Key Lab Visual Impairment & Restorat, Shanghai 200031, Peoples R China Fudan Univ, Eye & ENT Hosp, Eye Inst, Shanghai 200031, Peoples R ChinaHuo, Qiuyi论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Eye & ENT Hosp, Eye Inst, Shanghai 200031, Peoples R China Fudan Univ, Eye & ENT Hosp, Dept Ophthalmol, Shanghai 200031, Peoples R China Chinese Acad Med Sci, Key Lab Myopia Key Lab Myopia & Related Eye Dis, NHC, Shanghai 200031, Peoples R China Chinese Acad Med Sci, Key Lab Myopia & Related Eye Dis, Shanghai 200031, Peoples R China Shanghai Key Lab Visual Impairment & Restorat, Shanghai 200031, Peoples R China Fudan Univ, Eye & ENT Hosp, Eye Inst, Shanghai 200031, Peoples R ChinaSong, Linghao论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Eye & ENT Hosp, Eye Inst, Shanghai 200031, Peoples R China Fudan Univ, Eye & ENT Hosp, Dept Ophthalmol, Shanghai 200031, Peoples R China Chinese Acad Med Sci, Key Lab Myopia Key Lab Myopia & Related Eye Dis, NHC, Shanghai 200031, Peoples R China Chinese Acad Med Sci, Key Lab Myopia & Related Eye Dis, Shanghai 200031, Peoples R China Shanghai Key Lab Visual Impairment & Restorat, Shanghai 200031, Peoples R China Fudan Univ, Eye & ENT Hosp, Eye Inst, Shanghai 200031, Peoples R ChinaWang, Xinyue论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Eye & ENT Hosp, Eye Inst, Shanghai 200031, Peoples R China Fudan Univ, Eye & ENT Hosp, Dept Ophthalmol, Shanghai 200031, Peoples R China Chinese Acad Med Sci, Key Lab Myopia Key Lab Myopia & Related Eye Dis, NHC, Shanghai 200031, Peoples R China Chinese Acad Med Sci, Key Lab Myopia & Related Eye Dis, Shanghai 200031, Peoples R China Shanghai Key Lab Visual Impairment & Restorat, Shanghai 200031, Peoples R China Fudan Univ, Eye & ENT Hosp, Eye Inst, Shanghai 200031, Peoples R ChinaShen, Xin论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Eye & ENT Hosp, Eye Inst, Shanghai 200031, Peoples R China Fudan Univ, Eye & ENT Hosp, Dept Ophthalmol, Shanghai 200031, Peoples R China Chinese Acad Med Sci, Key Lab Myopia Key Lab Myopia & Related Eye Dis, NHC, Shanghai 200031, Peoples R China Chinese Acad Med Sci, Key Lab Myopia & Related Eye Dis, Shanghai 200031, Peoples R China Shanghai Key Lab Visual Impairment & Restorat, Shanghai 200031, Peoples R China Fudan Univ, Eye & ENT Hosp, Eye Inst, Shanghai 200031, Peoples R ChinaZhao, Ye论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Sch Basic Med Sci, Dept Physiol & Pathophysiol, Shanghai Key Lab Bioact Small Mol, Shanghai 200031, Peoples R China Fudan Univ, Eye & ENT Hosp, Eye Inst, Shanghai 200031, Peoples R ChinaChen, Tianhui论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Eye & ENT Hosp, Eye Inst, Shanghai 200031, Peoples R China Fudan Univ, Eye & ENT Hosp, Dept Ophthalmol, Shanghai 200031, Peoples R China Chinese Acad Med Sci, Key Lab Myopia Key Lab Myopia & Related Eye Dis, NHC, Shanghai 200031, Peoples R China Chinese Acad Med Sci, Key Lab Myopia & Related Eye Dis, Shanghai 200031, Peoples R China Shanghai Key Lab Visual Impairment & Restorat, Shanghai 200031, Peoples R China Fudan Univ, Eye & ENT Hosp, Eye Inst, Shanghai 200031, Peoples R ChinaJiang, Yongxiang论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Eye & ENT Hosp, Eye Inst, Shanghai 200031, Peoples R China Fudan Univ, Eye & ENT Hosp, Dept Ophthalmol, Shanghai 200031, Peoples R China Chinese Acad Med Sci, Key Lab Myopia Key Lab Myopia & Related Eye Dis, NHC, Shanghai 200031, Peoples R China Chinese Acad Med Sci, Key Lab Myopia & Related Eye Dis, Shanghai 200031, Peoples R China Shanghai Key Lab Visual Impairment & Restorat, Shanghai 200031, Peoples R China Fudan Univ, Eye & ENT Hosp, Eye Inst, Shanghai 200031, Peoples R China
- [10] Evidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type IMOLECULAR VISION, 2012, 18 (142-45): : 1379 - 1383Zhou, Qi论文数: 0 引用数: 0 h-index: 0机构: Peking Union Med Coll, Dept Ophthalmol, Beijing 100021, Peoples R China Peking Union Med Coll, Dept Ophthalmol, Beijing 100021, Peoples R ChinaLenger, Chaeli论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Genet Ctr, Omaha, NE USA Peking Union Med Coll, Dept Ophthalmol, Beijing 100021, Peoples R ChinaSmith, Richard论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Genet Ctr, Omaha, NE USA Peking Union Med Coll, Dept Ophthalmol, Beijing 100021, Peoples R ChinaKimberling, William J.论文数: 0 引用数: 0 h-index: 0机构: Boys Town Natl Res Hosp, Genet Ctr, Omaha, NE USA Peking Union Med Coll, Dept Ophthalmol, Beijing 100021, Peoples R ChinaYe, Ming论文数: 0 引用数: 0 h-index: 0机构: Univ Alberta, Dept Ophthalmol, Edmonton, AB T5H 3V9, Canada Univ Alberta, Dept Med Genet, Edmonton, AB T5H 3V9, Canada Peking Union Med Coll, Dept Ophthalmol, Beijing 100021, Peoples R China论文数: 引用数: h-index:机构:MacDonald, Ian论文数: 0 引用数: 0 h-index: 0机构: Univ Alberta, Dept Ophthalmol, Edmonton, AB T5H 3V9, Canada Univ Alberta, Dept Med Genet, Edmonton, AB T5H 3V9, Canada Peking Union Med Coll, Dept Ophthalmol, Beijing 100021, Peoples R China