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- [1] Identification of novel mutations by targeted exome sequencing and the genotype-phenotype assessment of patients with achromatopsiaJOURNAL OF TRANSLATIONAL MEDICINE, 2015, 13 : 1Li, Fen-Fen论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, State Key Lab Cultivat Base, Hosp Eye, Wenzhou 325027, Peoples R China Minist Hlth, Key Lab Vis Sci, Wenzhou 325027, Peoples R China Wenzhou Med Univ, State Key Lab Cultivat Base, Hosp Eye, Wenzhou 325027, Peoples R ChinaHuang, Xiu-Feng论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, State Key Lab Cultivat Base, Hosp Eye, Wenzhou 325027, Peoples R China Minist Hlth, Key Lab Vis Sci, Wenzhou 325027, Peoples R China Wenzhou Med Univ, State Key Lab Cultivat Base, Hosp Eye, Wenzhou 325027, Peoples R ChinaChen, Jie论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, State Key Lab Cultivat Base, Hosp Eye, Wenzhou 325027, Peoples R China Minist Hlth, Key Lab Vis Sci, Wenzhou 325027, Peoples R China Wenzhou Med Univ, State Key Lab Cultivat Base, Hosp Eye, Wenzhou 325027, Peoples R ChinaYu, Xu-Dong论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, State Key Lab Cultivat Base, Hosp Eye, Wenzhou 325027, Peoples R China Minist Hlth, Key Lab Vis Sci, Wenzhou 325027, Peoples R China Wenzhou Med Univ, State Key Lab Cultivat Base, Hosp Eye, Wenzhou 325027, Peoples R ChinaZheng, Mei-Qin论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, State Key Lab Cultivat Base, Hosp Eye, Wenzhou 325027, Peoples R China Minist Hlth, Key Lab Vis Sci, Wenzhou 325027, Peoples R China Wenzhou Med Univ, State Key Lab Cultivat Base, Hosp Eye, Wenzhou 325027, Peoples R ChinaLu, Fan论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, State Key Lab Cultivat Base, Hosp Eye, Wenzhou 325027, Peoples R China Minist Hlth, Key Lab Vis Sci, Wenzhou 325027, Peoples R China Wenzhou Med Univ, State Key Lab Cultivat Base, Hosp Eye, Wenzhou 325027, Peoples R ChinaJin, Zi-Bing论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, State Key Lab Cultivat Base, Hosp Eye, Wenzhou 325027, Peoples R China Minist Hlth, Key Lab Vis Sci, Wenzhou 325027, Peoples R China Wenzhou Med Univ, State Key Lab Cultivat Base, Hosp Eye, Wenzhou 325027, Peoples R ChinaGan, De-Kang论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Eye & ENT Hosp, Dept Ophthalmol, Shanghai 200031, Peoples R China Wenzhou Med Univ, State Key Lab Cultivat Base, Hosp Eye, Wenzhou 325027, Peoples R China
- [2] Genotype-phenotype analysis of 523 patients by genetics evaluation and clinical exome sequencingPEDIATRIC RESEARCH, 2020, 87 (04) : 735 - 739Ziats, Mark N.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Internal Med, Ann Arbor, MI USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USAAhmad, Ayesha论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Pediat, Div Pediat Genet Metab & Genom Med, Ann Arbor, MI 48109 USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USABernat, John A.论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa, Stead Family Dept Pediat, Div Med Genet, Iowa City, IA USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USAFisher, Rachel论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Pediat, Div Pediat Genet Metab & Genom Med, Ann Arbor, MI 48109 USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USAGlassford, Megan论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Pediat, Div Pediat Genet Metab & Genom Med, Ann Arbor, MI 48109 USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USAHannibal, Mark C.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Pediat, Div Pediat Genet Metab & Genom Med, Ann Arbor, MI 48109 USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USAJacher, Joseph E.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Pediat, Div Pediat Genet Metab & Genom Med, Ann Arbor, MI 48109 USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USAWeiser, Natasha论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Pediat, Div Pediat Genet Metab & Genom Med, Ann Arbor, MI 48109 USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USAKeegan, Catherine E.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Pediat, Div Pediat Genet Metab & Genom Med, Ann Arbor, MI 48109 USA Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA Univ Michigan, Childrens Clin Trial Support Unit, Ann Arbor, MI 48109 USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USALee, Kristen N.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Pediat, Div Pediat Genet Metab & Genom Med, Ann Arbor, MI 48109 USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USAMarzulla, Tessa B.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA Univ Michigan, Childrens Clin Trial Support Unit, Ann Arbor, MI 48109 USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USAO'Connor, Bridget C.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Pediat, Div Pediat Genet Metab & Genom Med, Ann Arbor, MI 48109 USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USAQuinonez, Shane C.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Internal Med, Ann Arbor, MI USA Univ Michigan, Dept Pediat, Div Pediat Genet Metab & Genom Med, Ann Arbor, MI 48109 USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USASeemann, Lauren论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA Univ Michigan, Childrens Clin Trial Support Unit, Ann Arbor, MI 48109 USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USATurner, Lauren论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA Univ Michigan, Childrens Clin Trial Support Unit, Ann Arbor, MI 48109 USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USA论文数: 引用数: h-index:机构:Harris, Nicholas L.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Childrens Clin Trial Support Unit, Ann Arbor, MI 48109 USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USAOgle, Jacob D.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Pediat, Div Pediat Genet Metab & Genom Med, Ann Arbor, MI 48109 USA Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA Univ Michigan, Childrens Clin Trial Support Unit, Ann Arbor, MI 48109 USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USAInnis, Jeffrey W.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Internal Med, Ann Arbor, MI USA Univ Michigan, Dept Pediat, Div Pediat Genet Metab & Genom Med, Ann Arbor, MI 48109 USA Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA Univ Michigan, Childrens Clin Trial Support Unit, Ann Arbor, MI 48109 USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USAMartin, Donna M.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Pediat, Div Pediat Genet Metab & Genom Med, Ann Arbor, MI 48109 USA Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA Univ Michigan, Childrens Clin Trial Support Unit, Ann Arbor, MI 48109 USA Univ Michigan, Dept Internal Med, Ann Arbor, MI USA
- [3] Genotype-phenotype relationship in patients affected by novel CLCNKB mutationsFASEB JOURNAL, 2013, 27Andrini, Olga论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 06, Paris, France Univ Paris 06, Paris, FranceKeck, Mathilde论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 06, Paris, France Univ Paris 06, Paris, FranceBlanchard, Anne论文数: 0 引用数: 0 h-index: 0机构: Hop Europeen Georges Pompidou, Paris, France Univ Paris 06, Paris, FranceVargas-Poussou, Rosa论文数: 0 引用数: 0 h-index: 0机构: Hop Europeen Georges Pompidou, Paris, France Univ Paris 06, Paris, FranceLourdel, Stephane论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 06, Paris, France Univ Paris 06, Paris, France论文数: 引用数: h-index:机构:
- [4] Identification of fifteen novel mutations and genotype-phenotype relationship in Fabry diseaseCLINICAL GENETICS, 2001, 60 (01) : 46 - 51Altarescu, GM论文数: 0 引用数: 0 h-index: 0机构: NINDS, Dev & Metab Neurol Branch, Bethesda, MD 20892 USAGoldfarb, LG论文数: 0 引用数: 0 h-index: 0机构: NINDS, Dev & Metab Neurol Branch, Bethesda, MD 20892 USAPark, KY论文数: 0 引用数: 0 h-index: 0机构: NINDS, Dev & Metab Neurol Branch, Bethesda, MD 20892 USAKaneski, C论文数: 0 引用数: 0 h-index: 0机构: NINDS, Dev & Metab Neurol Branch, Bethesda, MD 20892 USAJeffries, N论文数: 0 引用数: 0 h-index: 0机构: NINDS, Dev & Metab Neurol Branch, Bethesda, MD 20892 USALitvak, S论文数: 0 引用数: 0 h-index: 0机构: NINDS, Dev & Metab Neurol Branch, Bethesda, MD 20892 USANagle, JW论文数: 0 引用数: 0 h-index: 0机构: NINDS, Dev & Metab Neurol Branch, Bethesda, MD 20892 USASchiffmann, R论文数: 0 引用数: 0 h-index: 0机构: NINDS, Dev & Metab Neurol Branch, Bethesda, MD 20892 USA
- [5] Analysis of Genotype-Phenotype Correlations in Patients With Degenerative Dementia Through the Whole Exome SequencingFRONTIERS IN AGING NEUROSCIENCE, 2021, 13Sun, Lin论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R ChinaZhang, Jianye论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R ChinaSu, Ning论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R ChinaZhang, Shaowei论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R ChinaYan, Feng论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R ChinaLin, Xiang论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R ChinaYu, Jie论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R ChinaLi, Wei论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R ChinaLi, Xia论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R ChinaXiao, Shifu论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Dept Geriatr Psychiat, Alzheimers Dis & Related Disorders Ctr, Shanghai Mental Hlth Ctr,Sch Med, Shanghai, Peoples R China
- [6] The Value of Genotype-Phenotype Correlation in Research-Based Exome Sequencing of Epilepsy PatientsEPILEPSIA, 2018, 59 : S118 - S118Rochtus, A.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Epilepsy Genet Program, Dept Neurol, Boston, MA USA Boston Childrens Hosp, Epilepsy Genet Program, Dept Neurol, Boston, MA USAPark, M.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Epilepsy Genet Program, Dept Neurol, Boston, MA USA Boston Childrens Hosp, Epilepsy Genet Program, Dept Neurol, Boston, MA USASmith, L.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Epilepsy Genet Program, Dept Neurol, Boston, MA USA Boston Childrens Hosp, Epilepsy Genet Program, Dept Neurol, Boston, MA USATaylor, A.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Epilepsy Genet Program, Dept Neurol, Boston, MA USA Boston Childrens Hosp, Epilepsy Genet Program, Dept Neurol, Boston, MA USAEl Achkar, C.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Epilepsy Genet Program, Dept Neurol, Boston, MA USA Harvard Med Sch, Boston, MA USA Boston Childrens Hosp, Epilepsy Genet Program, Dept Neurol, Boston, MA USARockowitz, S.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Informat Serv Dept, Boston, MA USA Boston Childrens Hosp, Epilepsy Genet Program, Dept Neurol, Boston, MA USASheidley, B. R.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Epilepsy Genet Program, Dept Neurol, Boston, MA USA Boston Childrens Hosp, Epilepsy Genet Program, Dept Neurol, Boston, MA USAPoduri, A.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Epilepsy Genet Program, Dept Neurol, Boston, MA USA Harvard Med Sch, Boston, MA USA Boston Childrens Hosp, Epilepsy Genet Program, Dept Neurol, Boston, MA USA
- [7] Novel mutations and their genotype-phenotype correlations in patients with Noonan syndrome, using next-generation sequencingADVANCES IN MEDICAL SCIENCES, 2018, 63 (01): : 87 - 93论文数: 引用数: h-index:机构:Eshraghi, Peyman论文数: 0 引用数: 0 h-index: 0机构: Mashhad Univ Med Sci, Imam Reza Hosp, Dept Pediat, Mashhad, Iran Mashhad Univ Med Sci, Med Genet Res Ctr, Mashhad 9196773117, IranPantaleoni, Francesca论文数: 0 引用数: 0 h-index: 0机构: Ist Super Sanita, Dept Hematol Oncol & Mol Med, Rome, Italy IRCSS, Osped Pediat Bambino Gesu, Genet & Rare Dis, Res Ctr, Rome, Italy Mashhad Univ Med Sci, Med Genet Res Ctr, Mashhad 9196773117, IranVakili, Rahim论文数: 0 引用数: 0 h-index: 0机构: Mashhad Univ Med Sci, Imam Reza Hosp, Dept Pediat, Mashhad, Iran Mashhad Univ Med Sci, Med Genet Res Ctr, Mashhad 9196773117, IranMoghaddassian, Morteza论文数: 0 引用数: 0 h-index: 0机构: Univ Toronto, Fac Appl Sci & Engn, Edward S Rogers Sr Dept Elect & Comp Engn, Toronto, ON, Canada Mashhad Univ Med Sci, Med Genet Res Ctr, Mashhad 9196773117, IranGhahraman, Martha论文数: 0 引用数: 0 h-index: 0机构: Mashhad Univ Med Sci, Med Genet Res Ctr, Mashhad 9196773117, Iran Imam Reza Int Univ, Razavi Hosp, Razavi Canc Res Ctr, Mashhad, Iran Mashhad Univ Med Sci, Med Genet Res Ctr, Mashhad 9196773117, IranMuto, Valentina论文数: 0 引用数: 0 h-index: 0机构: Ist Super Sanita, Dept Hematol Oncol & Mol Med, Rome, Italy Mashhad Univ Med Sci, Med Genet Res Ctr, Mashhad 9196773117, IranPaolacci, Stefano论文数: 0 引用数: 0 h-index: 0机构: Ist Super Sanita, Dept Hematol Oncol & Mol Med, Rome, Italy Mashhad Univ Med Sci, Med Genet Res Ctr, Mashhad 9196773117, Iran论文数: 引用数: h-index:机构:Abbaszadegan, Mohammad Reza论文数: 0 引用数: 0 h-index: 0机构: Mashhad Univ Med Sci, Med Genet Res Ctr, Mashhad 9196773117, Iran Mashhad Univ Med Sci, Med Genet Res Ctr, Mashhad 9196773117, Iran
- [8] A REVIEW OF GENOTYPE-PHENOTYPE PRESENTATIONS IN PATIENTS WITH PSEUDOHYPOALDOSTERONISM TYPE 1 FOLLOWING THE IDENTIFICATION OF NOVEL MUTATIONSHORMONE RESEARCH IN PAEDIATRICS, 2017, 88 : 56 - 56Gopal-Kothandapani, Jaya Sujatha论文数: 0 引用数: 0 h-index: 0机构: Univ Sheffield, Sheffield, S Yorkshire, England Univ Sheffield, Sheffield, S Yorkshire, EnglandDoshi, Arpan论文数: 0 引用数: 0 h-index: 0机构: Sheffield Med Sch, Sheffield, S Yorkshire, England Univ Sheffield, Sheffield, S Yorkshire, EnglandMartin, Christian论文数: 0 引用数: 0 h-index: 0机构: Nottingham Univ Hosp, Nottingham, England Univ Sheffield, Sheffield, S Yorkshire, EnglandMushtaq, Talat论文数: 0 引用数: 0 h-index: 0机构: Leeds Teaching Hosp, Leeds, W Yorkshire, England Univ Sheffield, Sheffield, S Yorkshire, EnglandBanerjee, Indraneel论文数: 0 引用数: 0 h-index: 0机构: Cent Manchester Univ Hosp, Manchester, Lancs, England Univ Sheffield, Sheffield, S Yorkshire, EnglandPadidela, Raja论文数: 0 引用数: 0 h-index: 0机构: Royal Manchester Childrens Hosp, Manchester, Lancs, England Univ Sheffield, Sheffield, S Yorkshire, EnglandRamakrishnan, Renuka论文数: 0 引用数: 0 h-index: 0机构: Alder Hey Childrens Hosp, Liverpool, Merseyside, England Univ Sheffield, Sheffield, S Yorkshire, EnglandOwen, Catherine论文数: 0 引用数: 0 h-index: 0机构: Univ Sheffield, Sheffield, S Yorkshire, EnglandCheetham, Timothy论文数: 0 引用数: 0 h-index: 0机构: Royal Victoria Infirm, Newcastle, England Univ Sheffield, Sheffield, S Yorkshire, EnglandSmith, Kath论文数: 0 引用数: 0 h-index: 0机构: Sheffield Childrens Hosp, Sheffield, S Yorkshire, England Univ Sheffield, Sheffield, S Yorkshire, EnglandDimitri, Paul论文数: 0 引用数: 0 h-index: 0机构: Sheffield Childrens Hosp, Sheffield, S Yorkshire, England Univ Sheffield, Sheffield, S Yorkshire, England
- [9] A Genotype-Phenotype Correlation of Haemophilia a in Victorian Patients with a Description of Novel MutationsBLOOD, 2018, 132Sirdesai, Shreerang论文数: 0 引用数: 0 h-index: 0机构: Monash Hlth, Clayton, Vic, Australia Monash Hlth, Clayton, Vic, AustraliaWeekes, Kerryn论文数: 0 引用数: 0 h-index: 0机构: Monash Hlth, Clayton, Vic, Australia Monash Hlth, Clayton, Vic, AustraliaAlam, Asif论文数: 0 引用数: 0 h-index: 0机构: Monash Hlth, Clayton, Vic, Australia Monash Hlth, Clayton, Vic, AustraliaTran, Huyen A.论文数: 0 引用数: 0 h-index: 0机构: Alfred Hosp, Prahran, Vic, Australia Monash Hlth, Clayton, Vic, AustraliaBarnes, Christopher论文数: 0 引用数: 0 h-index: 0机构: Royal Childrens Hosp, Parkville, Vic, Australia Monash Hlth, Clayton, Vic, AustraliaKaplan, Zane论文数: 0 引用数: 0 h-index: 0机构: Monash Hlth, Clayton, Vic, Australia Australian Ctr Blood Dis, Melbourne, Vic, Australia Monash Hlth, Clayton, Vic, Australia
- [10] The Whole Exome Sequencing Clarifies the Genotype-Phenotype Correlations in Patients with Early-Onset DementiaAGING AND DISEASE, 2018, 9 (04): : 696 - 705Xu, Yangqi论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R ChinaLiu, Xiaoli论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Shanghai Fengxian Dist Cent Hosp, Dept Neurol, Affiliated Sixth Peoples Hosp South Campus, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R ChinaShen, Junyi论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R ChinaTian, Wotu论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R ChinaFang, Rong论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp North, Dept Neurol, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R ChinaLi, Binyin论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R ChinaMa, Jianfang论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R ChinaCao, Li论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R ChinaChen, Shengdi论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R ChinaLi, Guanjun论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Sch Med, Shanghai Mental Hlth Ctr, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R ChinaTang, Huidong论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai, Peoples R China