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- [41] Whole exome sequencing identifies a novel dominant missense mutation underlying leukonychia in a Pakistani familyJOURNAL OF HUMAN GENETICS, 2018, 63 (10) : 1071 - 1076Khan, Teka论文数: 0 引用数: 0 h-index: 0机构: USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R China USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R ChinaKhan, Manan论文数: 0 引用数: 0 h-index: 0机构: USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R China USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R ChinaYousaf, Ayesha论文数: 0 引用数: 0 h-index: 0机构: USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R China USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R China论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Shah, Akram论文数: 0 引用数: 0 h-index: 0机构: Univ Peshawar, Dept Zool, Peshawar, Pakistan USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R ChinaMurtaza, Ghulam论文数: 0 引用数: 0 h-index: 0机构: USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R China USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R ChinaAli, Asim论文数: 0 引用数: 0 h-index: 0机构: USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R China USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R ChinaJabeen, Nazish论文数: 0 引用数: 0 h-index: 0机构: USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R China USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R ChinaHussain, Hafiz Muhammad Jafar论文数: 0 引用数: 0 h-index: 0机构: USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R China USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R ChinaMa, Hui论文数: 0 引用数: 0 h-index: 0机构: USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R China USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R ChinaZhang, Yuanwei论文数: 0 引用数: 0 h-index: 0机构: USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R China USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R ChinaZubair, Muhammad论文数: 0 引用数: 0 h-index: 0机构: USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R China USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R ChinaJiang, Xiaohua论文数: 0 引用数: 0 h-index: 0机构: USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R China USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R ChinaZhang, Huan论文数: 0 引用数: 0 h-index: 0机构: USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R China USTC, CAS Ctr Excellence Mol Cell Sci,Collaborat Innova, USTC SJH Joint Ctr Human Reprod & Genet,Sch Life, CAS Key Lab Innate Immun & Chron Dis,Hefei Natl L, Hefei 230027, Anhui, Peoples R China
- [42] Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failureJOURNAL OF HUMAN GENETICS, 2013, 58 (05) : 259 - 266Izumi, Rumiko论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Dept Med Genet, Sch Med, Sendai, Miyagi 9808574, Japan Tohoku Univ, Dept Neurol, Sch Med, Sendai, Miyagi 9808574, Japan Tohoku Univ, Dept Med Genet, Sch Med, Sendai, Miyagi 9808574, Japan论文数: 引用数: h-index:机构:Aoki, Yoko论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Dept Med Genet, Sch Med, Sendai, Miyagi 9808574, Japan Tohoku Univ, Dept Med Genet, Sch Med, Sendai, Miyagi 9808574, JapanSuzuki, Naoki论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Dept Neurol, Sch Med, Sendai, Miyagi 9808574, Japan Tohoku Univ, Dept Med Genet, Sch Med, Sendai, Miyagi 9808574, JapanKato, Masaaki论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Dept Neurol, Sch Med, Sendai, Miyagi 9808574, Japan Tohoku Univ, Dept Med Genet, Sch Med, Sendai, Miyagi 9808574, JapanWarita, Hitoshi论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Dept Neurol, Sch Med, Sendai, Miyagi 9808574, Japan Tohoku Univ, Dept Med Genet, Sch Med, Sendai, Miyagi 9808574, JapanTakahashi, Toshiaki论文数: 0 引用数: 0 h-index: 0机构: Nishitaga Natl Hosp, Dept Neurol, Sendai, Miyagi, Japan Nishitaga Natl Hosp, Div Clin Res, Natl Hosp Org, Sendai, Miyagi, Japan Tohoku Univ, Dept Med Genet, Sch Med, Sendai, Miyagi 9808574, JapanTateyama, Maki论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Dept Neurol, Sch Med, Sendai, Miyagi 9808574, Japan Tohoku Univ, Dept Med Genet, Sch Med, Sendai, Miyagi 9808574, JapanNagashima, Takeshi论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Div Cell Proliferat, United Ctr Adv Res & Translat Med, Grad Sch Med, Sendai, Miyagi, Japan Tohoku Univ, Dept Med Genet, Sch Med, Sendai, Miyagi 9808574, JapanFunayama, Ryo论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Div Cell Proliferat, United Ctr Adv Res & Translat Med, Grad Sch Med, Sendai, Miyagi, Japan Tohoku Univ, Dept Med Genet, Sch Med, Sendai, Miyagi 9808574, JapanAbe, Koji论文数: 0 引用数: 0 h-index: 0机构: Okayama Univ, Sch Med, Dept Neurol, Okayama 700, Japan Tohoku Univ, Dept Med Genet, Sch Med, Sendai, Miyagi 9808574, JapanNakayama, Keiko论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Div Cell Proliferat, United Ctr Adv Res & Translat Med, Grad Sch Med, Sendai, Miyagi, Japan Tohoku Univ, Dept Med Genet, Sch Med, Sendai, Miyagi 9808574, JapanAoki, Masashi论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Dept Neurol, Sch Med, Sendai, Miyagi 9808574, Japan Tohoku Univ, Dept Med Genet, Sch Med, Sendai, Miyagi 9808574, JapanMatsubara, Yoichi论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Dept Med Genet, Sch Med, Sendai, Miyagi 9808574, Japan Tohoku Univ, Dept Med Genet, Sch Med, Sendai, Miyagi 9808574, Japan
- [43] Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failureJournal of Human Genetics, 2013, 58 : 259 - 266Rumiko Izumi论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsTetsuya Niihori论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsYoko Aoki论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsNaoki Suzuki论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsMasaaki Kato论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsHitoshi Warita论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsToshiaki Takahashi论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsMaki Tateyama论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsTakeshi Nagashima论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsRyo Funayama论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsKoji Abe论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsKeiko Nakayama论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsMasashi Aoki论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsYoichi Matsubara论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical Genetics
- [44] Exome Sequencing Identifies a Dominant TNNT3 Mutation in a Large Family with Distal ArthrogryposisMOLECULAR SYNDROMOLOGY, 2014, 5 (05) : 218 - 228Daly, Sarah B.论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, England Cent Manchester Univ Hosp NHS Fdn Trust, Manchester Ctr Genom Med, Manchester, Lancs, England Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, EnglandShah, Hitesh论文数: 0 引用数: 0 h-index: 0机构: Manipal Univ, Kasturba Med Coll, Dept Orthoped, Pediat Orthoped Serv, Manipal, India Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, EnglandO'Sullivan, James论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, England Cent Manchester Univ Hosp NHS Fdn Trust, Manchester Ctr Genom Med, Manchester, Lancs, England Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, EnglandAnderson, Beverley论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, England Cent Manchester Univ Hosp NHS Fdn Trust, Manchester Ctr Genom Med, Manchester, Lancs, England Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, EnglandBhaskar, Sanjeev论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, England Cent Manchester Univ Hosp NHS Fdn Trust, Manchester Ctr Genom Med, Manchester, Lancs, England Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, EnglandWilliams, Simon论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, England Cent Manchester Univ Hosp NHS Fdn Trust, Manchester Ctr Genom Med, Manchester, Lancs, England Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, EnglandAl-Sheqaih, Nada论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, England Cent Manchester Univ Hosp NHS Fdn Trust, Manchester Ctr Genom Med, Manchester, Lancs, England Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, EnglandBidchol, Abdul Mueed论文数: 0 引用数: 0 h-index: 0机构: Manipal Univ, Kasturba Med Coll, Dept Med Genet, Manipal 576104, India Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, EnglandBanka, Siddharth论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, England Cent Manchester Univ Hosp NHS Fdn Trust, Manchester Ctr Genom Med, Manchester, Lancs, England Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, EnglandNewman, William G.论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, England Cent Manchester Univ Hosp NHS Fdn Trust, Manchester Ctr Genom Med, Manchester, Lancs, England Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, EnglandGirisha, Katta M.论文数: 0 引用数: 0 h-index: 0机构: Manipal Univ, Kasturba Med Coll, Dept Med Genet, Manipal 576104, India Univ Manchester, Manchester Ctr Genom Med, Manchester, Lancs, England
- [45] Whole exome sequencing identifies a novel dominant missense mutation underlying leukonychia in a Pakistani familyJournal of Human Genetics, 2018, 63 : 1071 - 1076Teka Khan论文数: 0 引用数: 0 h-index: 0机构: University of Science and Technology of China (USTC),USTCManan Khan论文数: 0 引用数: 0 h-index: 0机构: University of Science and Technology of China (USTC),USTCAyesha Yousaf论文数: 0 引用数: 0 h-index: 0机构: University of Science and Technology of China (USTC),USTCSaadullah Khan论文数: 0 引用数: 0 h-index: 0机构: University of Science and Technology of China (USTC),USTCMuhammad Naeem论文数: 0 引用数: 0 h-index: 0机构: University of Science and Technology of China (USTC),USTCAkram Shah论文数: 0 引用数: 0 h-index: 0机构: University of Science and Technology of China (USTC),USTCGhulam Murtaza论文数: 0 引用数: 0 h-index: 0机构: University of Science and Technology of China (USTC),USTCAsim Ali论文数: 0 引用数: 0 h-index: 0机构: University of Science and Technology of China (USTC),USTCNazish Jabeen论文数: 0 引用数: 0 h-index: 0机构: University of Science and Technology of China (USTC),USTCHafiz Muhammad Jafar Hussain论文数: 0 引用数: 0 h-index: 0机构: University of Science and Technology of China (USTC),USTCHui Ma论文数: 0 引用数: 0 h-index: 0机构: University of Science and Technology of China (USTC),USTCYuanwei Zhang论文数: 0 引用数: 0 h-index: 0机构: University of Science and Technology of China (USTC),USTCMuhammad Zubair论文数: 0 引用数: 0 h-index: 0机构: University of Science and Technology of China (USTC),USTCXiaohua Jiang论文数: 0 引用数: 0 h-index: 0机构: University of Science and Technology of China (USTC),USTCHuan Zhang论文数: 0 引用数: 0 h-index: 0机构: University of Science and Technology of China (USTC),USTC
- [46] Whole-exome sequencing identifies a potential TTN mutation in a multiplex family with inguinal herniaHERNIA, 2017, 21 (01) : 95 - 100Mihailov, E.论文数: 0 引用数: 0 h-index: 0机构: Univ Tartu, Estonian Genome Ctr, 23b Riia St, EE-51010 Tartu, Estonia Univ Tartu, Estonian Genome Ctr, 23b Riia St, EE-51010 Tartu, EstoniaNikopensius, T.论文数: 0 引用数: 0 h-index: 0机构: Univ Tartu, Estonian Genome Ctr, 23b Riia St, EE-51010 Tartu, Estonia Univ Tartu, Estonian Genome Ctr, 23b Riia St, EE-51010 Tartu, EstoniaReigo, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Tartu, Estonian Genome Ctr, 23b Riia St, EE-51010 Tartu, Estonia Univ Tartu, Estonian Genome Ctr, 23b Riia St, EE-51010 Tartu, EstoniaNikkolo, C.论文数: 0 引用数: 0 h-index: 0机构: Tartu Univ Hosp, Surg Clin, 8 Puusepa St, EE-51014 Tartu, Estonia Univ Tartu, Estonian Genome Ctr, 23b Riia St, EE-51010 Tartu, EstoniaKals, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Tartu, Estonian Genome Ctr, 23b Riia St, EE-51010 Tartu, Estonia Univ Tartu, Estonian Genome Ctr, 23b Riia St, EE-51010 Tartu, EstoniaAruaas, K.论文数: 0 引用数: 0 h-index: 0机构: Univ Tartu, Inst Mol & Cell Biol, 23 Riia St, EE-51010 Tartu, Estonia Univ Tartu, Estonian Genome Ctr, 23b Riia St, EE-51010 Tartu, EstoniaMilani, L.论文数: 0 引用数: 0 h-index: 0机构: Univ Tartu, Estonian Genome Ctr, 23b Riia St, EE-51010 Tartu, Estonia Univ Tartu, Estonian Genome Ctr, 23b Riia St, EE-51010 Tartu, EstoniaSeepter, H.论文数: 0 引用数: 0 h-index: 0机构: Tartu Univ Hosp, Surg Clin, 8 Puusepa St, EE-51014 Tartu, Estonia Univ Tartu, Estonian Genome Ctr, 23b Riia St, EE-51010 Tartu, EstoniaMetspalu, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Tartu, Estonian Genome Ctr, 23b Riia St, EE-51010 Tartu, Estonia Univ Tartu, Inst Mol & Cell Biol, 23 Riia St, EE-51010 Tartu, Estonia Univ Tartu, Estonian Genome Ctr, 23b Riia St, EE-51010 Tartu, Estonia
- [47] Combinational analysis of linkage and exome sequencing identifies the causative mutation in a Chinese family with congenital cataractBMC MEDICAL GENETICS, 2013, 14Jia, Xueyuan论文数: 0 引用数: 0 h-index: 0机构: Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R China Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R ChinaZhang, Feng论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Sch Life Sci, Minist Educ, Key Lab Contemporary Anthropol, Shanghai 200433, Peoples R China Fudan Univ, Sch Life Sci, State Key Lab Genet Engn, Shanghai 200433, Peoples R China Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R ChinaBai, Jing论文数: 0 引用数: 0 h-index: 0机构: Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R China Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R ChinaGao, Linghan论文数: 0 引用数: 0 h-index: 0机构: Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R China Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R ChinaZhang, Xuelong论文数: 0 引用数: 0 h-index: 0机构: Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R China Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R ChinaSun, Haiming论文数: 0 引用数: 0 h-index: 0机构: Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R China Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R ChinaSun, Donglin论文数: 0 引用数: 0 h-index: 0机构: Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R China Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R ChinaGuan, Rongwei论文数: 0 引用数: 0 h-index: 0机构: Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R China Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R ChinaSun, Wenjing论文数: 0 引用数: 0 h-index: 0机构: Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R China Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R ChinaXu, Lidan论文数: 0 引用数: 0 h-index: 0机构: Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R China Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R ChinaYue, Zhichao论文数: 0 引用数: 0 h-index: 0机构: Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R China Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R ChinaYu, Yang论文数: 0 引用数: 0 h-index: 0机构: Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R China Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R ChinaFu, Songbin论文数: 0 引用数: 0 h-index: 0机构: Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R China Harbin Med Univ, Heilongjiang Higher Educ Inst, Key Lab Med Genet, Harbin 150081, Peoples R China Harbin Med Univ, Med Genet Lab, Harbin 150081, Peoples R China
- [48] ABCB4 mutation and intrahepatic cholestasis:: Cholesterol crystals in bile canaliculiLABORATORY INVESTIGATION, 2008, 88 : 317A - 318AWagner, B. E.论文数: 0 引用数: 0 h-index: 0机构: No Gen Hosp, Sheffield S5 7AU, S Yorkshire, EnglandStrautnieks, S. S.论文数: 0 引用数: 0 h-index: 0机构: No Gen Hosp, Sheffield S5 7AU, S Yorkshire, EnglandDevlin, J.论文数: 0 引用数: 0 h-index: 0机构: No Gen Hosp, Sheffield S5 7AU, S Yorkshire, EnglandDhawan, A.论文数: 0 引用数: 0 h-index: 0机构: No Gen Hosp, Sheffield S5 7AU, S Yorkshire, EnglandEdreessi, M. H.论文数: 0 引用数: 0 h-index: 0机构: No Gen Hosp, Sheffield S5 7AU, S Yorkshire, EnglandElferink, R. P. J. Oude论文数: 0 引用数: 0 h-index: 0机构: No Gen Hosp, Sheffield S5 7AU, S Yorkshire, EnglandThompson, R. J.论文数: 0 引用数: 0 h-index: 0机构: No Gen Hosp, Sheffield S5 7AU, S Yorkshire, EnglandKnisely, A. S.论文数: 0 引用数: 0 h-index: 0机构: No Gen Hosp, Sheffield S5 7AU, S Yorkshire, England
- [49] Lack of association of ABCB4 insertion mutation with gallbladder mucoceles in dogsJOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2014, 26 (03) : 434 - 436Cullen, John M.论文数: 0 引用数: 0 h-index: 0机构: N Carolina State Univ, Coll Vet Med, Dept Populat Hlth & Pathobiol, Raleigh, NC USA N Carolina State Univ, Coll Vet Med, Dept Populat Hlth & Pathobiol, Raleigh, NC USAWillson, Cynthia J.论文数: 0 引用数: 0 h-index: 0机构: N Carolina State Univ, Coll Vet Med, Dept Populat Hlth & Pathobiol, Raleigh, NC USA N Carolina State Univ, Coll Vet Med, Dept Populat Hlth & Pathobiol, Raleigh, NC USAMinch, Jonathan D.论文数: 0 引用数: 0 h-index: 0机构: Oregon State Univ, Hatfield Marine Sci Ctr, Newport, OR 97365 USA N Carolina State Univ, Coll Vet Med, Dept Populat Hlth & Pathobiol, Raleigh, NC USAKimbrough, Carie L.论文数: 0 引用数: 0 h-index: 0机构: GlaxoSmithKline, Res Triangle Pk, NC USA N Carolina State Univ, Coll Vet Med, Dept Populat Hlth & Pathobiol, Raleigh, NC USAMealey, Katrina L.论文数: 0 引用数: 0 h-index: 0机构: Washington State Univ, Coll Vet Med, Dept Vet Clin Sci, Pullman, WA 99164 USA N Carolina State Univ, Coll Vet Med, Dept Populat Hlth & Pathobiol, Raleigh, NC USA
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