共 50 条
- [1] MN1 gene loss-of-function mutation causes cleft palate in a pedigreeBRAIN, 2021, 144Shu, Li论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Hunan Prov, Dept Med Genet, Changsha, Peoples R China Hunan Prov Maternal & Child Hlth Care Hosp, Natl Hlth Commiss, Key Lab Birth Defects Res Prevent & Treatment, Changsha, Peoples R China Cent South Univ, Dept Sch Life Sci, Changsha, Peoples R China Maternal & Child Hlth Hosp Hunan Prov, Dept Med Genet, Changsha, Peoples R ChinaHe, Dinghua论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Hunan Prov, Dept Otorhinolaryngol, Changsha, Peoples R China Maternal & Child Hlth Hosp Hunan Prov, Dept Med Genet, Changsha, Peoples R ChinaWu, Dan论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Hunan Prov, Dept Otorhinolaryngol, Changsha, Peoples R China Maternal & Child Hlth Hosp Hunan Prov, Dept Med Genet, Changsha, Peoples R ChinaPeng, Ying论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Hunan Prov, Dept Med Genet, Changsha, Peoples R China Maternal & Child Hlth Hosp Hunan Prov, Dept Med Genet, Changsha, Peoples R ChinaXi, Hui论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Hunan Prov, Dept Med Genet, Changsha, Peoples R China Maternal & Child Hlth Hosp Hunan Prov, Dept Med Genet, Changsha, Peoples R ChinaMao, Xiao论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Hunan Prov, Dept Med Genet, Changsha, Peoples R China Hunan Prov Maternal & Child Hlth Care Hosp, Natl Hlth Commiss, Key Lab Birth Defects Res Prevent & Treatment, Changsha, Peoples R China Maternal & Child Hlth Hosp Hunan Prov, Dept Med Genet, Changsha, Peoples R ChinaWang, Hua论文数: 0 引用数: 0 h-index: 0机构: Maternal & Child Hlth Hosp Hunan Prov, Dept Med Genet, Changsha, Peoples R China Hunan Prov Maternal & Child Hlth Care Hosp, Natl Hlth Commiss, Key Lab Birth Defects Res Prevent & Treatment, Changsha, Peoples R China Maternal & Child Hlth Hosp Hunan Prov, Dept Med Genet, Changsha, Peoples R China
- [2] Reply: MN1 gene loss-of-function mutation causes cleft palate in a pedigreeBRAIN, 2021, 144 (02)Vegas, Nancy论文数: 0 引用数: 0 h-index: 0机构: Univ Paris, Inst Natl Sante & Rech Med INSERM, Inst Imagine, Lab Embryol & Genet Human Malformat,UMR 1163, F-75015 Paris, France Univ Paris, Inst Natl Sante & Rech Med INSERM, Inst Imagine, Lab Embryol & Genet Human Malformat,UMR 1163, F-75015 Paris, FranceLow, Karen论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Bristol & Weston NHS Trust, St Michaels Hosp, Dept Clin Genet, Bristol BS2 8EJ, England Univ Paris, Inst Natl Sante & Rech Med INSERM, Inst Imagine, Lab Embryol & Genet Human Malformat,UMR 1163, F-75015 Paris, FranceMak, Christopher C. Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Hong Kong, Peoples R China Univ Paris, Inst Natl Sante & Rech Med INSERM, Inst Imagine, Lab Embryol & Genet Human Malformat,UMR 1163, F-75015 Paris, FranceFung, Jasmine L. F.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Hong Kong, Peoples R China Univ Paris, Inst Natl Sante & Rech Med INSERM, Inst Imagine, Lab Embryol & Genet Human Malformat,UMR 1163, F-75015 Paris, FranceHing, Anne V.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Div Craniofacial Med, Dept Pediat, Seattle, WA 98195 USA Seattle Childrens Hosp, Seattle Craniofacial Ctr, Seattle, WA 98105 USA Univ Paris, Inst Natl Sante & Rech Med INSERM, Inst Imagine, Lab Embryol & Genet Human Malformat,UMR 1163, F-75015 Paris, FranceChung, Brian H. Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Hong Kong, Peoples R China Univ Paris, Inst Natl Sante & Rech Med INSERM, Inst Imagine, Lab Embryol & Genet Human Malformat,UMR 1163, F-75015 Paris, France论文数: 引用数: h-index:机构:Amiel, Jeanne论文数: 0 引用数: 0 h-index: 0机构: Univ Paris, Inst Natl Sante & Rech Med INSERM, Inst Imagine, Lab Embryol & Genet Human Malformat,UMR 1163, F-75015 Paris, France Hop Necker Enfants Malad, Assistance Publ Hop Paris AP HP, Dept Genet, F-75015 Paris, France Univ Paris, Inst Natl Sante & Rech Med INSERM, Inst Imagine, Lab Embryol & Genet Human Malformat,UMR 1163, F-75015 Paris, FranceGordon, Christopher T.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris, Inst Natl Sante & Rech Med INSERM, Inst Imagine, Lab Embryol & Genet Human Malformat,UMR 1163, F-75015 Paris, France Univ Paris, Inst Natl Sante & Rech Med INSERM, Inst Imagine, Lab Embryol & Genet Human Malformat,UMR 1163, F-75015 Paris, France
- [3] Reply: MN1 gene loss-of-function mutation causes cleft palate in a pedigreeBRAIN, 2021, 144Vegas, Nancy论文数: 0 引用数: 0 h-index: 0机构: Univ Paris, Inst Natl Sante & Rech Medicale INSERM UMR 1163, Inst Imagine, Lab Embryol & Genet Human Malformat, F-75015 Paris, France Univ Paris, Inst Natl Sante & Rech Medicale INSERM UMR 1163, Inst Imagine, Lab Embryol & Genet Human Malformat, F-75015 Paris, FranceLow, Karen论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Bristol & Weston NHS Trust, St Michaels Hosp, Dept Clin Genet, Bristol BS2 8EJ, Avon, England Univ Paris, Inst Natl Sante & Rech Medicale INSERM UMR 1163, Inst Imagine, Lab Embryol & Genet Human Malformat, F-75015 Paris, FranceMak, Christopher C. Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Hong Kong, Peoples R China Univ Paris, Inst Natl Sante & Rech Medicale INSERM UMR 1163, Inst Imagine, Lab Embryol & Genet Human Malformat, F-75015 Paris, FranceFung, Jasmine L. F.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Hong Kong, Peoples R China Univ Paris, Inst Natl Sante & Rech Medicale INSERM UMR 1163, Inst Imagine, Lab Embryol & Genet Human Malformat, F-75015 Paris, FranceHing, Anne V.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Div Craniofacial Med, Dept Pediat, Seattle, WA 98195 USA Seattle Childrens Hosp, Seattle Craniofacial Ctr, Seattle, WA 98105 USA Univ Paris, Inst Natl Sante & Rech Medicale INSERM UMR 1163, Inst Imagine, Lab Embryol & Genet Human Malformat, F-75015 Paris, FranceChung, Brian H. Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, LKS Fac Med, Dept Paediat & Adolescent Med, Hong Kong, Peoples R China Univ Paris, Inst Natl Sante & Rech Medicale INSERM UMR 1163, Inst Imagine, Lab Embryol & Genet Human Malformat, F-75015 Paris, France论文数: 引用数: h-index:机构:Amiel, Jeanne论文数: 0 引用数: 0 h-index: 0机构: Univ Paris, Inst Natl Sante & Rech Medicale INSERM UMR 1163, Inst Imagine, Lab Embryol & Genet Human Malformat, F-75015 Paris, France Hop Necker Enfants Malad, AP HP, Dept Genet, F-75015 Paris, France Univ Paris, Inst Natl Sante & Rech Medicale INSERM UMR 1163, Inst Imagine, Lab Embryol & Genet Human Malformat, F-75015 Paris, FranceGordon, Christopher T.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris, Inst Natl Sante & Rech Medicale INSERM UMR 1163, Inst Imagine, Lab Embryol & Genet Human Malformat, F-75015 Paris, France Univ Paris, Inst Natl Sante & Rech Medicale INSERM UMR 1163, Inst Imagine, Lab Embryol & Genet Human Malformat, F-75015 Paris, France
- [4] Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palateEUROPEAN JOURNAL OF HUMAN GENETICS, 2016, 24 (01) : 51 - 58Breckpot, Jeroen论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, Belgium Katholieke Univ Leuven, Dept Human Genet, Leuven, Belgium Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, BelgiumAnderlid, Britt-Marie论文数: 0 引用数: 0 h-index: 0机构: Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, BelgiumAlanay, Yasemin论文数: 0 引用数: 0 h-index: 0机构: Acibadem Univ, Sch Med, Dept Pediat, Pediat Genet Unit, Istanbul, Turkey Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, BelgiumBlyth, Moira论文数: 0 引用数: 0 h-index: 0机构: Chapel Allerton Hosp, Yorkshire Reg Genet Serv, Leeds, W Yorkshire, England Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, BelgiumBrahimi, Afane论文数: 0 引用数: 0 h-index: 0机构: GHICL, Hop St Vincent de Paul, Ctr Genet Chromosom, Lille, France Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, BelgiumDuban-Bedu, Benedicte论文数: 0 引用数: 0 h-index: 0机构: GHICL, Hop St Vincent de Paul, Ctr Genet Chromosom, Lille, France Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, BelgiumGoze, Odile论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Valenciennes, Serv Pediat, Valenciennes, France Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, BelgiumFirth, Helen论文数: 0 引用数: 0 h-index: 0机构: Addenbrookes Hosp, East Anglian Med Genet Serv, Dept Clin Genet, Cambridge, England Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, BelgiumYakicier, Mustafa Cengiz论文数: 0 引用数: 0 h-index: 0机构: Acibadem Univ, Dept Mol Biol & Genet, Istanbul, Turkey Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, BelgiumHens, Greet论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Leuven, ENT Dept, B-3000 Leuven, Belgium Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, BelgiumRayyan, Maissa论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Leuven, Neonatol Unit, B-3000 Leuven, Belgium Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, BelgiumLegius, Eric论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, Belgium Katholieke Univ Leuven, Dept Human Genet, Leuven, Belgium Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, BelgiumVermeesch, Joris Robert论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, Belgium Katholieke Univ Leuven, Dept Human Genet, Leuven, Belgium Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, BelgiumDevriendt, Koen论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, Belgium Katholieke Univ Leuven, Dept Human Genet, Leuven, Belgium Univ Hosp Leuven, Ctr Human Genet, B-3000 Leuven, Belgium
- [5] Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palateEuropean Journal of Human Genetics, 2016, 24 : 51 - 58Jeroen Breckpot论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,University Hospitals Leuven and Department of Human GeneticsBritt-Marie Anderlid论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,University Hospitals Leuven and Department of Human GeneticsYasemin Alanay论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,University Hospitals Leuven and Department of Human GeneticsMoira Blyth论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,University Hospitals Leuven and Department of Human GeneticsAfane Brahimi论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,University Hospitals Leuven and Department of Human GeneticsBénédicte Duban-Bedu论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,University Hospitals Leuven and Department of Human GeneticsOdile Gozé论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,University Hospitals Leuven and Department of Human GeneticsHelen Firth论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,University Hospitals Leuven and Department of Human GeneticsMustafa Cengiz Yakicier论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,University Hospitals Leuven and Department of Human GeneticsGreet Hens论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,University Hospitals Leuven and Department of Human GeneticsMaissa Rayyan论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,University Hospitals Leuven and Department of Human GeneticsEric Legius论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,University Hospitals Leuven and Department of Human GeneticsJoris Robert Vermeesch论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,University Hospitals Leuven and Department of Human GeneticsKoen Devriendt论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,University Hospitals Leuven and Department of Human Genetics
- [6] HAND1 Loss-of-Function Mutation Causes Tetralogy of FallotPediatric Cardiology, 2017, 38 : 547 - 557Juan Wang论文数: 0 引用数: 0 h-index: 0机构: Tongji University School of Medicine,Department of Cardiovascular Medicine, East HospitalXiao-Qing Hu论文数: 0 引用数: 0 h-index: 0机构: Tongji University School of Medicine,Department of Cardiovascular Medicine, East HospitalYu-Han Guo论文数: 0 引用数: 0 h-index: 0机构: Tongji University School of Medicine,Department of Cardiovascular Medicine, East HospitalJian-Yun Gu论文数: 0 引用数: 0 h-index: 0机构: Tongji University School of Medicine,Department of Cardiovascular Medicine, East HospitalJia-Hong Xu论文数: 0 引用数: 0 h-index: 0机构: Tongji University School of Medicine,Department of Cardiovascular Medicine, East HospitalYan-Jie Li论文数: 0 引用数: 0 h-index: 0机构: Tongji University School of Medicine,Department of Cardiovascular Medicine, East HospitalNing Li论文数: 0 引用数: 0 h-index: 0机构: Tongji University School of Medicine,Department of Cardiovascular Medicine, East HospitalXiao-Xiao Yang论文数: 0 引用数: 0 h-index: 0机构: Tongji University School of Medicine,Department of Cardiovascular Medicine, East HospitalYi-Qing Yang论文数: 0 引用数: 0 h-index: 0机构: Tongji University School of Medicine,Department of Cardiovascular Medicine, East Hospital
- [7] HAND1 Loss-of-Function Mutation Causes Tetralogy of FallotPEDIATRIC CARDIOLOGY, 2017, 38 (03) : 547 - 557Wang, Juan论文数: 0 引用数: 0 h-index: 0机构: Tongji Univ, Sch Med, East Hosp, Dept Cardiovasc Med, Shanghai 200120, Peoples R China Tongji Univ, Sch Med, East Hosp, Dept Cardiovasc Med, Shanghai 200120, Peoples R ChinaHu, Xiao-Qing论文数: 0 引用数: 0 h-index: 0机构: Tongji Univ, Sch Med, East Hosp, Dept Cardiovasc Med, Shanghai 200120, Peoples R China Tongji Univ, Sch Med, East Hosp, Dept Cardiovasc Med, Shanghai 200120, Peoples R ChinaGuo, Yu-Han论文数: 0 引用数: 0 h-index: 0机构: Tongji Univ, Sch Med, Tongji Hosp, Dept Cardiol, Shanghai 200065, Peoples R China Tongji Univ, Sch Med, East Hosp, Dept Cardiovasc Med, Shanghai 200120, Peoples R ChinaGu, Jian-Yun论文数: 0 引用数: 0 h-index: 0机构: Tongji Univ, Sch Med, Tongji Hosp, Dept Cardiol, Shanghai 200065, Peoples R China Tongji Univ, Sch Med, East Hosp, Dept Cardiovasc Med, Shanghai 200120, Peoples R ChinaXu, Jia-Hong论文数: 0 引用数: 0 h-index: 0机构: Tongji Univ, Sch Med, Tongji Hosp, Dept Cardiol, Shanghai 200065, Peoples R China Tongji Univ, Sch Med, East Hosp, Dept Cardiovasc Med, Shanghai 200120, Peoples R ChinaLi, Yan-Jie论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Dept Cardiol, Shanghai 200030, Peoples R China Tongji Univ, Sch Med, East Hosp, Dept Cardiovasc Med, Shanghai 200120, Peoples R ChinaLi, Ning论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Dept Cardiol, Shanghai 200030, Peoples R China Tongji Univ, Sch Med, East Hosp, Dept Cardiovasc Med, Shanghai 200120, Peoples R ChinaYang, Xiao-Xiao论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Dept Cardiol, Shanghai 200030, Peoples R China Tongji Univ, Sch Med, East Hosp, Dept Cardiovasc Med, Shanghai 200120, Peoples R ChinaYang, Yi-Qing论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Dept Cardiol, Shanghai 200030, Peoples R China Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Dept Cardiovasc Res Lab, Shanghai 200030, Peoples R China Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Dept Cent Lab, Shanghai 200030, Peoples R China Tongji Univ, Sch Med, East Hosp, Dept Cardiovasc Med, Shanghai 200120, Peoples R China
- [8] A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis, and cleft palateJOURNAL OF MEDICAL GENETICS, 2002, 39 : S21 - S21Park, SM论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Addenbrookes Hosp, Dept Med, Cambridge CB2 2QQ, EnglandCastanet, M论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Addenbrookes Hosp, Dept Med, Cambridge CB2 2QQ, EnglandSmith, A论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Addenbrookes Hosp, Dept Med, Cambridge CB2 2QQ, EnglandBost, M论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Addenbrookes Hosp, Dept Med, Cambridge CB2 2QQ, EnglandLeger, J论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Addenbrookes Hosp, Dept Med, Cambridge CB2 2QQ, EnglandLyonnet, S论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Addenbrookes Hosp, Dept Med, Cambridge CB2 2QQ, EnglandCzemichow, P论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Addenbrookes Hosp, Dept Med, Cambridge CB2 2QQ, EnglandChatterjee, K论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Addenbrookes Hosp, Dept Med, Cambridge CB2 2QQ, EnglandPolak, M论文数: 0 引用数: 0 h-index: 0机构: Univ Cambridge, Addenbrookes Hosp, Dept Med, Cambridge CB2 2QQ, England
- [9] A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palateHUMAN MOLECULAR GENETICS, 2002, 11 (17) : 2051 - 2059Castanet, M论文数: 0 引用数: 0 h-index: 0机构: Paediat Endocrinol Unit, Paris, FrancePark, SM论文数: 0 引用数: 0 h-index: 0机构: Paediat Endocrinol Unit, Paris, FranceSmith, A论文数: 0 引用数: 0 h-index: 0机构: Paediat Endocrinol Unit, Paris, FranceBost, M论文数: 0 引用数: 0 h-index: 0机构: Paediat Endocrinol Unit, Paris, FranceLéger, J论文数: 0 引用数: 0 h-index: 0机构: Paediat Endocrinol Unit, Paris, FranceLyonnet, S论文数: 0 引用数: 0 h-index: 0机构: Paediat Endocrinol Unit, Paris, FrancePelet, A论文数: 0 引用数: 0 h-index: 0机构: Paediat Endocrinol Unit, Paris, FranceCzernichow, P论文数: 0 引用数: 0 h-index: 0机构: Paediat Endocrinol Unit, Paris, FranceChatterjee, K论文数: 0 引用数: 0 h-index: 0机构: Paediat Endocrinol Unit, Paris, FrancePolak, M论文数: 0 引用数: 0 h-index: 0机构: Paediat Endocrinol Unit, Paris, France
- [10] Identification of a novel loss-of-function missense mutation in the RANKL gene that causes osteopetrosis in miceCALCIFIED TISSUE INTERNATIONAL, 2008, 82 : S57 - S57Douni, E.论文数: 0 引用数: 0 h-index: 0机构: BSRC Alexander Fleming, Inst Immunol, Vari, Greece BSRC Alexander Fleming, Inst Immunol, Vari, GreeceMakrinou, E.论文数: 0 引用数: 0 h-index: 0机构: BSRC Alexander Fleming, Inst Immunol, Vari, Greece BSRC Alexander Fleming, Inst Immunol, Vari, GreeceKollias, G.论文数: 0 引用数: 0 h-index: 0机构: BSRC Alexander Fleming, Inst Immunol, Vari, Greece BSRC Alexander Fleming, Inst Immunol, Vari, Greece