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- [1] Copy number variants are frequent in genetic generalized epilepsy with intellectual disability (vol 81, pg 2148, 2013)[J]. NEUROLOGY, 2014, 82 (05) : 462 - 462Mullen, Saul A.论文数: 0 引用数: 0 h-index: 0
- [2] Copy number variants are frequent in genetic generalized epilepsy with intellectual disability[J]. NEUROLOGY, 2013, 81 (17) : 1507 - 1514Mullen, Saul A.论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Melbourne, Vic 3010, Australia Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Melbourne, Vic 3010, AustraliaCarvill, Gemma L.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Pediat, Div Med Genet, Seattle, WA 98195 USA Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Melbourne, Vic 3010, AustraliaBellows, Susannah论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Austin & Northern Hlth, Dept Med, Epilepsy Res Ctr, Melbourne, Vic 3010, Australia Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Melbourne, Vic 3010, AustraliaBayly, Marta A.论文数: 0 引用数: 0 h-index: 0机构: Univ S Australia, Epilepsy Res Program, Sch Pharm & Med Sci, Adelaide, SA 5001, Australia Univ S Australia, Sansom Inst Hlth Res, Adelaide, SA 5001, Australia Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Melbourne, Vic 3010, AustraliaBerkovic, Samuel F.论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Austin & Northern Hlth, Dept Med, Epilepsy Res Ctr, Melbourne, Vic 3010, Australia Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Melbourne, Vic 3010, AustraliaDibbens, Leanne M.论文数: 0 引用数: 0 h-index: 0机构: Univ S Australia, Epilepsy Res Program, Sch Pharm & Med Sci, Adelaide, SA 5001, Australia Univ S Australia, Sansom Inst Hlth Res, Adelaide, SA 5001, Australia Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Melbourne, Vic 3010, AustraliaScheffer, Ingrid E.论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Melbourne, Vic 3010, Australia Univ Melbourne, Austin & Northern Hlth, Dept Med, Epilepsy Res Ctr, Melbourne, Vic 3010, Australia Univ Melbourne, Royal Childrens Hosp, Dept Paediat, Melbourne, Vic 3010, Australia Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Melbourne, Vic 3010, AustraliaMefford, Heather C.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Pediat, Div Med Genet, Seattle, WA 98195 USA Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Melbourne, Vic 3010, Australia
- [3] The epilepsy phenotype in adult patients with intellectual disability and pathogenic copy number variants[J]. SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2017, 53 : 86 - 93d'Orsi, Giuseppe论文数: 0 引用数: 0 h-index: 0机构: Riuniti Hosp, Clin Nervous Syst Dis, Epilepsy Ctr, Foggia, Italy Riuniti Hosp, Clin Nervous Syst Dis, Epilepsy Ctr, Foggia, ItalyMartino, Tommaso论文数: 0 引用数: 0 h-index: 0机构: Riuniti Hosp, Clin Nervous Syst Dis, Epilepsy Ctr, Foggia, Italy Riuniti Hosp, Clin Nervous Syst Dis, Epilepsy Ctr, Foggia, ItalyPalumbo, Orazio论文数: 0 引用数: 0 h-index: 0机构: IRCCS Casa Sollievo Sofferenza, Med Genet Units, Foggia, Italy Riuniti Hosp, Clin Nervous Syst Dis, Epilepsy Ctr, Foggia, ItalyPascarella, Maria Grazia论文数: 0 引用数: 0 h-index: 0机构: Riuniti Hosp, Clin Nervous Syst Dis, Epilepsy Ctr, Foggia, Italy Riuniti Hosp, Clin Nervous Syst Dis, Epilepsy Ctr, Foggia, ItalyPalumbo, Pietro论文数: 0 引用数: 0 h-index: 0机构: IRCCS Casa Sollievo Sofferenza, Med Genet Units, Foggia, Italy Riuniti Hosp, Clin Nervous Syst Dis, Epilepsy Ctr, Foggia, ItalyDi Claudio, Maria Teresa论文数: 0 引用数: 0 h-index: 0机构: Riuniti Hosp, Clin Nervous Syst Dis, Epilepsy Ctr, Foggia, Italy Riuniti Hosp, Clin Nervous Syst Dis, Epilepsy Ctr, Foggia, ItalyAvolio, Carlo论文数: 0 引用数: 0 h-index: 0机构: Riuniti Hosp, Clin Nervous Syst Dis, Epilepsy Ctr, Foggia, Italy Riuniti Hosp, Clin Nervous Syst Dis, Epilepsy Ctr, Foggia, ItalyCarella, Massimo论文数: 0 引用数: 0 h-index: 0机构: IRCCS Casa Sollievo Sofferenza, Med Genet Units, Foggia, Italy Riuniti Hosp, Clin Nervous Syst Dis, Epilepsy Ctr, Foggia, Italy
- [4] Copy number variations in Saudi family with intellectual disability and epilepsy[J]. BMC GENOMICS, 2015, 17Naseer, Muhammad I.论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaChaudhary, Adeel G.论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaRasool, Mahmood论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaKalamegam, Gauthaman论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaAshgan, Fai T.论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaAssidi, Mourad论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaAhmed, Farid论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaAnsari, Shakeel A.论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaZaidi, Syed Kashif论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaJan, Mohammed M.论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Fac Med, Dept Pediat, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi ArabiaAl-Qahtani, Mohammad H.论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah 21589, Saudi Arabia
- [5] Prevalence of copy number variation in adults with epilepsy and intellectual disability[J]. NEUROLOGY, 2017, 88Borlot, Felippe论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Sch Med, Dept Neurol, Salt Lake City, UT USA Univ Utah, Sch Med, Dept Neurol, Salt Lake City, UT USABassett, Anne论文数: 0 引用数: 0 h-index: 0机构: Dept Psychiat, Toronto, ON, Canada Univ Utah, Sch Med, Dept Neurol, Salt Lake City, UT USARegan, Brigid论文数: 0 引用数: 0 h-index: 0机构: Toronto Western Hosp, Toronto, ON, Canada Univ Utah, Sch Med, Dept Neurol, Salt Lake City, UT USAStavropoulos, James论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Toronto, ON, Canada Univ Utah, Sch Med, Dept Neurol, Salt Lake City, UT USAAndrade, Danielle论文数: 0 引用数: 0 h-index: 0机构: Univ Toronto, Div Neurol, Toronto, ON, Canada Univ Utah, Sch Med, Dept Neurol, Salt Lake City, UT USA
- [6] Copy number variations in Saudi family with intellectual disability and epilepsy[J]. BMC Genomics, 17Muhammad I. Naseer论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchAdeel G. Chaudhary论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchMahmood Rasool论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchGauthaman Kalamegam论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchFai T. Ashgan论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchMourad Assidi论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchFarid Ahmed论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchShakeel A. Ansari论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchSyed Kashif Zaidi论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchMohammed M. Jan论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine ResearchMohammad H. Al-Qahtani论文数: 0 引用数: 0 h-index: 0机构: King Abdulaziz University,Center of Excellence in Genomic Medicine Research
- [7] Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia[J]. JAMA PSYCHIATRY, 2016, 73 (09) : 963 - 969Rees, Elliott论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, Wales Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, WalesKendall, Kimberley论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, Wales Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, WalesPardinas, Antonio F.论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, Wales Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, WalesLegge, Sophie E.论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, Wales Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, WalesPocklington, Andrew论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, Wales Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, WalesEscott-Price, Valentina论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, Wales Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, WalesMacCabe, James H.论文数: 0 引用数: 0 h-index: 0机构: Kings Coll London, Dept Psychosis Studies, Inst Psychiat Psychol & Neurosci, London, England Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, WalesCollier, David A.论文数: 0 引用数: 0 h-index: 0机构: Kings Coll London, SGDP Ctr, Inst Psychiat Psychol & Neurosci, London, England Eli Lilly & Co Ltd, Lilly Res Labs, Discovery Neurosci Res, Surrey, England Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, WalesHolmans, Peter论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, Wales Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, WalesO'Donovan, Michael C.论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, Wales Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, WalesOwen, Michael J.论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, Wales Cardiff Univ, Div Psychol Med & Clin Neurosci, Cardiff, S Glam, Wales Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, WalesWalters, James T. R.论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, Wales Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, WalesKirov, George论文数: 0 引用数: 0 h-index: 0机构: Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, Wales Cardiff Univ, Med Res Council, Ctr Neuropsychiat Genet & Genom, Hadyn Ellis Bldg,Maindy Rd, Cardiff CF24 4HQ, S Glam, Wales
- [8] COPY NUMBER VARIANTS LINKED TO INTELLECTUAL DISABILITY, LESS EDUCATION[J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2015, 167 (09) : VIII - IX不详论文数: 0 引用数: 0 h-index: 0
- [9] Rare Copy Number Variations and Predictors in Children With Intellectual Disability and Epilepsy[J]. FRONTIERS IN NEUROLOGY, 2018, 9论文数: 引用数: h-index:机构:Xiong, Juan论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R ChinaWu, Liwen论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R ChinaYang, Lifen论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R ChinaHe, Fang论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China论文数: 引用数: h-index:机构:Pang, Nan论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R ChinaDuan, Haolin论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R ChinaZhang, Wen论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R ChinaArafat, Ahmed论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R ChinaYin, Fei论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R ChinaPeng, Jing论文数: 0 引用数: 0 h-index: 0机构: Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent S Univ, Xiangya Hosp, Dept Pediat, Changsha, Hunan, Peoples R China
- [10] Characterization of copy number variants identified by genetic testing of epilepsy[J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 490 - 490Koskinen, Lotta论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandHathaway, Julie论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandAlakurtti, Kirsi论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandCastell, Monica Segura论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandHagstrom, Asa论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandKuisma, Heli论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandGall, Kimberly论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandSaarinen, Inka论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandMuona, Mikko论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandPietila, Tuuli论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandDjupsjobacka, Janica论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandGentile, Massimiliano论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandSalmenpera, Pertteli论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandTuupanen, Sari论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandKangas-Kontio, Tiia论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandKampjarvi, Kati论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandSeppala, Eija H.论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandPaananen, Jussi论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandMyllykangas, Samuel论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, FinlandKoskenvuo, Juha论文数: 0 引用数: 0 h-index: 0机构: Quest Diagnost Co, Blueprint Genet, Espoo, Finland Quest Diagnost Co, Blueprint Genet, Espoo, Finland