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- [1] Loss-of-Function Mutations in HPSE2 Cause the Autosomal Recessive Urofacial SyndromeAMERICAN JOURNAL OF HUMAN GENETICS, 2010, 86 (06) : 957 - 962Pang, Junfeng论文数: 0 引用数: 0 h-index: 0机构: Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USA Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USAZhang, Shu论文数: 0 引用数: 0 h-index: 0机构: Huazhong Univ Sci & Technol, Ctr Biomed Res, Tongji Hosp, Tongji Med Coll, Wuhan 430030, Peoples R China Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USAYang, Ping论文数: 0 引用数: 0 h-index: 0机构: Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USA Huazhong Univ Sci & Technol, Ctr Biomed Res, Tongji Hosp, Tongji Med Coll, Wuhan 430030, Peoples R China Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USAHawkins-Lee, Bobbilynn论文数: 0 引用数: 0 h-index: 0机构: Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USA Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USAZhong, Jixin论文数: 0 引用数: 0 h-index: 0机构: Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USA Huazhong Univ Sci & Technol, Ctr Biomed Res, Tongji Hosp, Tongji Med Coll, Wuhan 430030, Peoples R China Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USAZhang, Yushan论文数: 0 引用数: 0 h-index: 0机构: Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USA Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USAOchoa, Bernardo论文数: 0 引用数: 0 h-index: 0机构: Univ Antioquia, Dept Pediat Surg, Univ Hosp San Vincente de Paul, Medellin 90827, Colombia Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USAAgundez, Jose A. G.论文数: 0 引用数: 0 h-index: 0机构: Univ Extremadura, Sch Med, Dept Pharmacol, Badajoz 06006, Spain Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USAVoelckel, Marie-Antoinette论文数: 0 引用数: 0 h-index: 0机构: Hosp Enfants Timone, Dept Med Genet, F-13001 Marseille, France Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USAGu, Weikuan论文数: 0 引用数: 0 h-index: 0机构: Univ Tennessee, Hlth Sci Ctr, Dept Orthopaed Surg Campbell Clin & Pathol, Memphis, TN 38104 USA Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USAXiong, Wen-Cheng论文数: 0 引用数: 0 h-index: 0机构: Med Coll Georgia, Inst Mol Med & Genet, Augusta, GA 30912 USA Med Coll Georgia, Dept Neurol, Augusta, GA 30912 USA Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USAMei, Lin论文数: 0 引用数: 0 h-index: 0机构: Med Coll Georgia, Inst Mol Med & Genet, Augusta, GA 30912 USA Med Coll Georgia, Dept Neurol, Augusta, GA 30912 USA Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USAShe, Jin-Xiong论文数: 0 引用数: 0 h-index: 0机构: Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USA Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USAWang, Cong-Yi论文数: 0 引用数: 0 h-index: 0机构: Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USA Med Coll Georgia, Dept Pathol, Augusta, GA 30912 USA Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USA
- [2] Mutations in HPSE2 Cause Urofacial Syndrome (vol 86, pg 963, 2010)AMERICAN JOURNAL OF HUMAN GENETICS, 2010, 87 (02) : 309 - 309Daly, Sarah B.论文数: 0 引用数: 0 h-index: 0Urquhart, Jill E.论文数: 0 引用数: 0 h-index: 0Hilton, Emma论文数: 0 引用数: 0 h-index: 0McKenzie, Edward A.论文数: 0 引用数: 0 h-index: 0Kammerer, Richard A.论文数: 0 引用数: 0 h-index: 0Lewis, Malcolm论文数: 0 引用数: 0 h-index: 0Kerr, Bronwyn论文数: 0 引用数: 0 h-index: 0Stuart, Helen论文数: 0 引用数: 0 h-index: 0Donnai, Dian论文数: 0 引用数: 0 h-index: 0Long, David A.论文数: 0 引用数: 0 h-index: 0Burgu, Berk论文数: 0 引用数: 0 h-index: 0Aydogdu, Ozgu论文数: 0 引用数: 0 h-index: 0Derbent, Murat论文数: 0 引用数: 0 h-index: 0Garcia-Minaur, Sixto论文数: 0 引用数: 0 h-index: 0Reardon, Willie论文数: 0 引用数: 0 h-index: 0Gener, Blanca论文数: 0 引用数: 0 h-index: 0Shalev, Stavit论文数: 0 引用数: 0 h-index: 0Smith, Rupert论文数: 0 引用数: 0 h-index: 0Woolf, Adrian S.论文数: 0 引用数: 0 h-index: 0Black, Graeme C.论文数: 0 引用数: 0 h-index: 0Newman, William G.论文数: 0 引用数: 0 h-index: 0
- [3] Mutations in HPSE2 cause urofacial syndromeJOURNAL OF MEDICAL GENETICS, 2010, 47 : S27 - S27Daly, Sarah论文数: 0 引用数: 0 h-index: 0机构: St Marys Hosp, Manchester, Lancs, England St Marys Hosp, Manchester, Lancs, EnglandUrquhart, J. E.论文数: 0 引用数: 0 h-index: 0机构: St Marys Hosp, Manchester, Lancs, England St Marys Hosp, Manchester, Lancs, EnglandStuart, H.论文数: 0 引用数: 0 h-index: 0机构: St Marys Hosp, Manchester, Lancs, England St Marys Hosp, Manchester, Lancs, EnglandLewis, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Sch Biomed, Manchester M13 9PL, Lancs, England St Marys Hosp, Manchester, Lancs, EnglandKerr, B.论文数: 0 引用数: 0 h-index: 0机构: St Marys Hosp, Manchester, Lancs, England St Marys Hosp, Manchester, Lancs, EnglandDonnai, D.论文数: 0 引用数: 0 h-index: 0机构: St Marys Hosp, Manchester, Lancs, England St Marys Hosp, Manchester, Lancs, EnglandWoolf, A. S.论文数: 0 引用数: 0 h-index: 0机构: St Marys Hosp, Manchester, Lancs, England St Marys Hosp, Manchester, Lancs, EnglandBlack, G. C.论文数: 0 引用数: 0 h-index: 0机构: St Marys Hosp, Manchester, Lancs, England St Marys Hosp, Manchester, Lancs, EnglandNewman, W. G.论文数: 0 引用数: 0 h-index: 0机构: St Marys Hosp, Manchester, Lancs, England St Marys Hosp, Manchester, Lancs, England
- [4] Mutations in HPSE2 Cause Urofacial SyndromeAMERICAN JOURNAL OF HUMAN GENETICS, 2010, 86 (06) : 963 - 969Daly, Sarah B.论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, England Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandUrquhart, Jill E.论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, England Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandHilton, Emma论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, England Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandMcKenzie, Edward A.论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Fac Life Sci, Prot Express Facil, Manchester M13 9PT, Lancs, England Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandKammerer, Richard A.论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Fac Life Sci, Wellcome Trust Ctr Cell Matrix Res, Manchester M13 9PT, Lancs, England Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandLewis, Malcolm论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Dept Paediat, Cent Manchester Fdn Natl Hlth Serv NHS Trust, Sch Biomed, Manchester M13 9WL, Lancs, England Univ Manchester, Sch Biomed, Regenerat Med Res Grp, Manchester M13 9WL, Lancs, England Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandKerr, Bronwyn论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, England Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandStuart, Helen论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, England Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandDonnai, Dian论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, England Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandLong, David A.论文数: 0 引用数: 0 h-index: 0机构: UCL Inst Child Hlth, Nephrourol Unit, London WC1N 1EH, England Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, England论文数: 引用数: h-index:机构:Aydogdu, Ozgu论文数: 0 引用数: 0 h-index: 0机构: Ankara Univ, Sch Med, Div Paediat Urol, TR-06100 Ankara, Turkey Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandDerbent, Murat论文数: 0 引用数: 0 h-index: 0机构: Baskent Univ, Fac Med, Dept Paediat, TR-06490 Ankara, Turkey Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandGarcia-Minaur, Sixto论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp La Paz, Inst Med & Mol Genet, Madrid 28046, Spain Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandReardon, Willie论文数: 0 引用数: 0 h-index: 0机构: Our Ladys Hosp Sick Children, Natl Ctr Med Genet, Dublin 12, Ireland Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandGener, Blanca论文数: 0 引用数: 0 h-index: 0机构: Hosp Cruces, Baracaldo 48903, Vizcaya, Spain Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandShalev, Stavit论文数: 0 引用数: 0 h-index: 0机构: HaEmek Med Ctr, Inst Genet, IL-18101 Afula, Israel Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandSmith, Rupert论文数: 0 引用数: 0 h-index: 0机构: Pennine Acute Hosp NHS Trust, Rochdale Infirm, Rochdale OL12 0NB, England Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandWoolf, Adrian S.论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Dept Paediat, Cent Manchester Fdn Natl Hlth Serv NHS Trust, Sch Biomed, Manchester M13 9WL, Lancs, England Univ Manchester, Sch Biomed, Regenerat Med Res Grp, Manchester M13 9WL, Lancs, England Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandBlack, Graeme C.论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, England Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, EnglandNewman, William G.论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, England Univ Manchester, Sch Biomed, MAHSC, St Marys Hosp, Manchester M13 9WL, Lancs, England
- [5] Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing lossHuman Genetics, 2020, 139 : 1565 - 1574Kevin T. Booth论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyAmama Ghaffar论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyMuhammad Rashid论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyLuke T. Hovey论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyMureed Hussain论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyKathy Frees论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyErika M. Renkes论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyCarla J. Nishimura论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyMohsin Shahzad论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyRichard J. Smith论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyZubair Ahmed论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologyHela Azaiez论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of OtolaryngologySaima Riazuddin论文数: 0 引用数: 0 h-index: 0机构: University of Iowa,Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology
- [6] ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfectaHUMAN MOLECULAR GENETICS, 2014, 23 (08) : 2157 - 2163Wang, Shih-Kai论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Biol & Mat Sci, Sch Dent, Ann Arbor, MI 48108 USA Univ Michigan, Oral Hlth Sci Program, Sch Dent, Ann Arbor, MI 48109 USA Univ Michigan, Dept Biol & Mat Sci, Sch Dent, Ann Arbor, MI 48108 USAChoi, Murim论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Dept Biomed Sci, Coll Med, Seoul 110768, South Korea Yale Univ, Sch Med, Dept Genet, Howard Hughes Med Inst, New Haven, CT 06520 USA Univ Michigan, Dept Biol & Mat Sci, Sch Dent, Ann Arbor, MI 48108 USARichardson, Amelia S.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Biol & Mat Sci, Sch Dent, Ann Arbor, MI 48108 USA Univ Michigan, Dept Biol & Mat Sci, Sch Dent, Ann Arbor, MI 48108 USAReid, Bryan M.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Biol & Mat Sci, Sch Dent, Ann Arbor, MI 48108 USA Univ Michigan, Dept Biol & Mat Sci, Sch Dent, Ann Arbor, MI 48108 USALin, Brent P.论文数: 0 引用数: 0 h-index: 0机构: UCSF, Sch Dent, Dept Orofacial Sci, San Francisco, CA 94143 USA Univ Michigan, Dept Biol & Mat Sci, Sch Dent, Ann Arbor, MI 48108 USAWang, Susan J.论文数: 0 引用数: 0 h-index: 0机构: Friends Family Hlth Ctr, La Habra, CA 90631 USA Univ Michigan, Dept Biol & Mat Sci, Sch Dent, Ann Arbor, MI 48108 USAKim, Jung-Wook论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Dept Pediat Dent, Sch Dent, Seoul 110768, South Korea Seoul Natl Univ, Dent Res Inst, Sch Dent, Seoul 110768, South Korea Univ Michigan, Dept Biol & Mat Sci, Sch Dent, Ann Arbor, MI 48108 USASimmer, James P.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Biol & Mat Sci, Sch Dent, Ann Arbor, MI 48108 USA Univ Michigan, Dept Biol & Mat Sci, Sch Dent, Ann Arbor, MI 48108 USAHu, Jan C. -C.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Dept Biol & Mat Sci, Sch Dent, Ann Arbor, MI 48108 USA Univ Michigan, Dept Biol & Mat Sci, Sch Dent, Ann Arbor, MI 48108 USA
- [7] Analysis Of Hpse2 Gene Mutations In Children With Non-neurogenic Neurogenic Bladder And Urofacial (ochoa) SyndromePEDIATRIC NEPHROLOGY, 2014, 29 (09) : 1698 - 1698Bulum, Burcu论文数: 0 引用数: 0 h-index: 0机构: Ankara Univ, Sch Med, Dept Pediat Nephrol, TR-06100 Ankara, Turkey Ankara Univ, Sch Med, Dept Pediat Nephrol, TR-06100 Ankara, TurkeyOzCakar, Z. Birsin论文数: 0 引用数: 0 h-index: 0机构: Ankara Univ, Sch Med, Dept Pediat Nephrol, TR-06100 Ankara, Turkey Ankara Univ, Sch Med, Dept Pediat Nephrol, TR-06100 Ankara, TurkeyDuman, Duygu论文数: 0 引用数: 0 h-index: 0机构: Ankara Univ, Sch Med, Dept Pediat Genet, TR-06100 Ankara, Turkey Ankara Univ, Sch Med, Dept Pediat Nephrol, TR-06100 Ankara, TurkeyCengiz, Filiz BaSak论文数: 0 引用数: 0 h-index: 0机构: Ankara Univ, Sch Med, Dept Pediat Genet, TR-06100 Ankara, Turkey Ankara Univ, Sch Med, Dept Pediat Nephrol, TR-06100 Ankara, Turkey论文数: 引用数: h-index:机构:Baskin, Esra论文数: 0 引用数: 0 h-index: 0机构: Baskent Univ, Sch Med, Dept Pediat Nephrol, TR-06490 Ankara, Turkey Ankara Univ, Sch Med, Dept Pediat Nephrol, TR-06100 Ankara, TurkeyCakar, NilgUn论文数: 0 引用数: 0 h-index: 0机构: Ankara Pediat & Pediat Hematol Oncol Training & R, Dept Pediat Nephrol, Ankara, Turkey Ankara Univ, Sch Med, Dept Pediat Nephrol, TR-06100 Ankara, TurkeySoygUr, Tarkan论文数: 0 引用数: 0 h-index: 0机构: Ankara Univ, Sch Med, Dept Pediat Urol, TR-06100 Ankara, Turkey Ankara Univ, Sch Med, Dept Pediat Nephrol, TR-06100 Ankara, TurkeyEkim, Mesiha论文数: 0 引用数: 0 h-index: 0机构: Ankara Univ, Sch Med, Dept Pediat Nephrol, TR-06100 Ankara, Turkey Ankara Univ, Sch Med, Dept Pediat Nephrol, TR-06100 Ankara, TurkeyTekin, Mustafa论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Miller Sch Med, Dept Human Genet, Miami, FL 33136 USA Univ Miami, Miller Sch Med, Hussman Inst Human Genom, Miami, FL 33136 USA Ankara Univ, Sch Med, Dept Pediat Nephrol, TR-06100 Ankara, TurkeyYalCinkaya, FatoS论文数: 0 引用数: 0 h-index: 0机构: Ankara Univ, Sch Med, Dept Pediat Nephrol, TR-06100 Ankara, Turkey Ankara Univ, Sch Med, Dept Pediat Nephrol, TR-06100 Ankara, Turkey
- [8] Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndromeJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2008, 93 (10): : 4113 - 4118Abreu, Ana Paula论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Hosp Clin,Disciplina Endocrinol & Metab, Fac Med,Dev Endocrinol Unit, Sch Med,Lab Hormone, BR-05403900 Sao Paulo, Brazil Univ Sao Paulo, Hosp Clin,Disciplina Endocrinol & Metab, Fac Med,Dev Endocrinol Unit, Sch Med,Lab Hormone, BR-05403900 Sao Paulo, BrazilTrarbach, Ericka Barbosa论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Hosp Clin,Disciplina Endocrinol & Metab, Fac Med,Dev Endocrinol Unit, Sch Med,Lab Hormone, BR-05403900 Sao Paulo, Brazil Univ Sao Paulo, Hosp Clin,Disciplina Endocrinol & Metab, Fac Med,Dev Endocrinol Unit, Sch Med,Lab Hormone, BR-05403900 Sao Paulo, Brazilde Castro, Margaret论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Med Sch Ribeirao Preto, Clin Hosp, Dept Internal Med, BR-14049900 Ribeirao Preto, Brazil Univ Sao Paulo, Hosp Clin,Disciplina Endocrinol & Metab, Fac Med,Dev Endocrinol Unit, Sch Med,Lab Hormone, BR-05403900 Sao Paulo, BrazilFrade Costa, Elaine Maria论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Hosp Clin,Disciplina Endocrinol & Metab, Fac Med,Dev Endocrinol Unit, Sch Med,Lab Hormone, BR-05403900 Sao Paulo, Brazil Univ Sao Paulo, Hosp Clin,Disciplina Endocrinol & Metab, Fac Med,Dev Endocrinol Unit, Sch Med,Lab Hormone, BR-05403900 Sao Paulo, BrazilVersiani, Beatriz论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Med Sch Ribeirao Preto, Clin Hosp, Dept Internal Med, BR-14049900 Ribeirao Preto, Brazil Univ Sao Paulo, Hosp Clin,Disciplina Endocrinol & Metab, Fac Med,Dev Endocrinol Unit, Sch Med,Lab Hormone, BR-05403900 Sao Paulo, BrazilMatias Baptista, Maria Tereza论文数: 0 引用数: 0 h-index: 0机构: Univ Estadual Campinas, Clin Hosp, Dept Internal Med, BR-13083970 Campinas, SP, Brazil Univ Sao Paulo, Hosp Clin,Disciplina Endocrinol & Metab, Fac Med,Dev Endocrinol Unit, Sch Med,Lab Hormone, BR-05403900 Sao Paulo, BrazilGarmes, Heraldo Mendes论文数: 0 引用数: 0 h-index: 0机构: Univ Estadual Campinas, Clin Hosp, Dept Internal Med, BR-13083970 Campinas, SP, Brazil Univ Sao Paulo, Hosp Clin,Disciplina Endocrinol & Metab, Fac Med,Dev Endocrinol Unit, Sch Med,Lab Hormone, BR-05403900 Sao Paulo, BrazilMendonca, Berenice Bilharinho论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Hosp Clin,Disciplina Endocrinol & Metab, Fac Med,Dev Endocrinol Unit, Sch Med,Lab Hormone, BR-05403900 Sao Paulo, Brazil Univ Sao Paulo, Hosp Clin,Disciplina Endocrinol & Metab, Fac Med,Dev Endocrinol Unit, Sch Med,Lab Hormone, BR-05403900 Sao Paulo, BrazilLatronico, Ana Claudia论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Hosp Clin,Disciplina Endocrinol & Metab, Fac Med,Dev Endocrinol Unit, Sch Med,Lab Hormone, BR-05403900 Sao Paulo, Brazil Univ Sao Paulo, Hosp Clin,Disciplina Endocrinol & Metab, Fac Med,Dev Endocrinol Unit, Sch Med,Lab Hormone, BR-05403900 Sao Paulo, Brazil
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