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- [1] Genotype-phenotype correlations in recessive RYR1-related myopathiesOrphanet Journal of Rare Diseases, 8Kimberly Amburgey论文数: 0 引用数: 0 h-index: 0机构: University of Michigan Medical Center,Department of Pediatrics, Taubman Medical Research InstituteAngela Bailey论文数: 0 引用数: 0 h-index: 0机构: University of Michigan Medical Center,Department of Pediatrics, Taubman Medical Research InstituteJean H Hwang论文数: 0 引用数: 0 h-index: 0机构: University of Michigan Medical Center,Department of Pediatrics, Taubman Medical Research InstituteMark A Tarnopolsky论文数: 0 引用数: 0 h-index: 0机构: University of Michigan Medical Center,Department of Pediatrics, Taubman Medical Research InstituteCarsten G Bonnemann论文数: 0 引用数: 0 h-index: 0机构: University of Michigan Medical Center,Department of Pediatrics, Taubman Medical Research InstituteLivija Medne论文数: 0 引用数: 0 h-index: 0机构: University of Michigan Medical Center,Department of Pediatrics, Taubman Medical Research InstituteKatherine D Mathews论文数: 0 引用数: 0 h-index: 0机构: University of Michigan Medical Center,Department of Pediatrics, Taubman Medical Research InstituteJames Collins论文数: 0 引用数: 0 h-index: 0机构: University of Michigan Medical Center,Department of Pediatrics, Taubman Medical Research InstituteJasper R Daube论文数: 0 引用数: 0 h-index: 0机构: University of Michigan Medical Center,Department of Pediatrics, Taubman Medical Research InstituteGregory P Wellman论文数: 0 引用数: 0 h-index: 0机构: University of Michigan Medical Center,Department of Pediatrics, Taubman Medical Research InstituteBrian Callaghan论文数: 0 引用数: 0 h-index: 0机构: University of Michigan Medical Center,Department of Pediatrics, Taubman Medical Research InstituteNigel F Clarke论文数: 0 引用数: 0 h-index: 0机构: University of Michigan Medical Center,Department of Pediatrics, Taubman Medical Research InstituteJames J Dowling论文数: 0 引用数: 0 h-index: 0机构: University of Michigan Medical Center,Department of Pediatrics, Taubman Medical Research Institute
- [2] Genotype-phenotype correlations in recessive RYR1-related myopathiesORPHANET JOURNAL OF RARE DISEASES, 2013, 8Amburgey, Kimberly论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Ctr Med, Dept Pediat, Taubman Med Res Inst, Ann Arbor, MI 48109 USA Univ Michigan, Ctr Med, Dept Pediat, Taubman Med Res Inst, Ann Arbor, MI 48109 USA论文数: 引用数: h-index:机构:Hwang, Jean H.论文数: 0 引用数: 0 h-index: 0机构: Univ Sydney, Childrens Hosp Westmead, Inst Neurosci & Muscle Res, Sydney, NSW 2145, Australia Univ Michigan, Ctr Med, Dept Pediat, Taubman Med Res Inst, Ann Arbor, MI 48109 USATarnopolsky, Mark A.论文数: 0 引用数: 0 h-index: 0机构: McMaster Univ, Med Ctr, Dept Neuromuscular & Neurometabol Dis, Hamilton, ON, Canada Univ Michigan, Ctr Med, Dept Pediat, Taubman Med Res Inst, Ann Arbor, MI 48109 USABonnemann, Carsten G.论文数: 0 引用数: 0 h-index: 0机构: NIH, Neuromuscular & Neurogenet Disorders Childhood Se, Bethesda, MD 20892 USA Univ Michigan, Ctr Med, Dept Pediat, Taubman Med Res Inst, Ann Arbor, MI 48109 USAMedne, Livija论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USA Univ Michigan, Ctr Med, Dept Pediat, Taubman Med Res Inst, Ann Arbor, MI 48109 USAMathews, Katherine D.论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa, Dept Pediat, Carver Coll Med, Iowa City, IA 52242 USA Univ Iowa, Dept Neurol, Carver Coll Med, Iowa City, IA 52242 USA Univ Michigan, Ctr Med, Dept Pediat, Taubman Med Res Inst, Ann Arbor, MI 48109 USACollins, James论文数: 0 引用数: 0 h-index: 0机构: Cincinnati Childrens Hosp Med Ctr, Dept Pediat Neurol, Cincinnati, OH 45229 USA Univ Michigan, Ctr Med, Dept Pediat, Taubman Med Res Inst, Ann Arbor, MI 48109 USADaube, Jasper R.论文数: 0 引用数: 0 h-index: 0机构: Mayo Fdn Med Educ & Res, Dept Neurol, Rochester, MN USA Univ Michigan, Ctr Med, Dept Pediat, Taubman Med Res Inst, Ann Arbor, MI 48109 USAWellman, Gregory P.论文数: 0 引用数: 0 h-index: 0机构: Delta Pathol Grp, Shreveport, LA USA Univ Michigan, Ctr Med, Dept Pediat, Taubman Med Res Inst, Ann Arbor, MI 48109 USACallaghan, Brian论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Med Ctr, Dept Neurol, Ann Arbor, MI 48109 USA Univ Michigan, Ctr Med, Dept Pediat, Taubman Med Res Inst, Ann Arbor, MI 48109 USAClarke, Nigel F.论文数: 0 引用数: 0 h-index: 0机构: Univ Sydney, Childrens Hosp Westmead, Inst Neurosci & Muscle Res, Sydney, NSW 2145, Australia Univ Sydney, Discipline Paediat & Child Hlth, Sydney, NSW 2145, Australia Univ Michigan, Ctr Med, Dept Pediat, Taubman Med Res Inst, Ann Arbor, MI 48109 USADowling, James J.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Ctr Med, Dept Pediat, Taubman Med Res Inst, Ann Arbor, MI 48109 USA Univ Michigan, Ctr Med, Dept Pediat, Taubman Med Res Inst, Ann Arbor, MI 48109 USA
- [3] Genotype-phenotype correlations in recessive RYR1-related myopathiesNEUROMUSCULAR DISORDERS, 2014, 24 (9-10) : 809 - 809Amburgey, K.论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Toronto, ON M5G 1X8, Canada Hosp Sick Children, Toronto, ON M5G 1X8, CanadaBailey, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Ann Arbor, MI 48109 USA Hosp Sick Children, Toronto, ON M5G 1X8, CanadaHwang, J. H.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Westmead, Sydney, NSW, Australia Hosp Sick Children, Toronto, ON M5G 1X8, CanadaTamopolsky, M. A.论文数: 0 引用数: 0 h-index: 0机构: McMaster Univ, Med Ctr, Hamilton, ON, Canada Hosp Sick Children, Toronto, ON M5G 1X8, CanadaBoennemann, C. G.论文数: 0 引用数: 0 h-index: 0机构: NIH, Bethesda, MD 20892 USA Hosp Sick Children, Toronto, ON M5G 1X8, CanadaMedne, L.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA Hosp Sick Children, Toronto, ON M5G 1X8, CanadaMathews, K. D.论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa, Carver Coll Med, Iowa City, IA USA Hosp Sick Children, Toronto, ON M5G 1X8, CanadaCollins, J.论文数: 0 引用数: 0 h-index: 0机构: Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USA Hosp Sick Children, Toronto, ON M5G 1X8, CanadaDaube, J. R.论文数: 0 引用数: 0 h-index: 0机构: Mayo Fdn Med Educ & Res, Rochester, MN USA Hosp Sick Children, Toronto, ON M5G 1X8, CanadaWellman, G. P.论文数: 0 引用数: 0 h-index: 0机构: Delta Pathol Grp, Shreveport, LA USA Hosp Sick Children, Toronto, ON M5G 1X8, CanadaCallaghan, B.论文数: 0 引用数: 0 h-index: 0机构: Univ Michigan, Med Ctr, Ann Arbor, MI USA Hosp Sick Children, Toronto, ON M5G 1X8, CanadaVajsar, J.论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Toronto, ON M5G 1X8, Canada Hosp Sick Children, Toronto, ON M5G 1X8, CanadaYoon, G.论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Toronto, ON M5G 1X8, Canada Hosp Sick Children, Toronto, ON M5G 1X8, CanadaCohn, R.论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Toronto, ON M5G 1X8, Canada Hosp Sick Children, Toronto, ON M5G 1X8, CanadaClarke, N. F.论文数: 0 引用数: 0 h-index: 0机构: Univ Sydney, Sydney, NSW 2006, Australia Hosp Sick Children, Toronto, ON M5G 1X8, CanadaDowling, J. J.论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Toronto, ON M5G 1X8, Canada Hosp Sick Children, Toronto, ON M5G 1X8, Canada
- [4] Novel SPEG mutations in congenital myopathies: Genotype-phenotype correlationsMUSCLE & NERVE, 2019, 59 (03) : 357 - 362Qualls, Anita E.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Genet & Gen, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USA Boston Childrens Hosp, Manton Ctr Orphan Dis Res, 300 Longwood Ave, Boston, MA 02115 USA Harvard Med Sch, 300 Longwood Ave, Boston, MA 02115 USA Boston Childrens Hosp, Div Genet & Gen, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USADonkervoort, Sandra论文数: 0 引用数: 0 h-index: 0机构: NIH, Neuromuscular & Neurogenet Disorders Childhood, Bldg 10, Bethesda, MD 20892 USA Boston Childrens Hosp, Div Genet & Gen, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USAHerkert, Johanna C.论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands Boston Childrens Hosp, Div Genet & Gen, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USAD'gama, Alissa M.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Genet & Gen, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USA Boston Childrens Hosp, Manton Ctr Orphan Dis Res, 300 Longwood Ave, Boston, MA 02115 USA Harvard Med Sch, 300 Longwood Ave, Boston, MA 02115 USA Boston Childrens Hosp, Div Genet & Gen, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USABharucha-Goebel, Diana论文数: 0 引用数: 0 h-index: 0机构: NIH, Neuromuscular & Neurogenet Disorders Childhood, Bldg 10, Bethesda, MD 20892 USA Childrens Natl Hlth Syst, Div Neurol, Washington, DC USA Boston Childrens Hosp, Div Genet & Gen, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USACollins, James论文数: 0 引用数: 0 h-index: 0机构: Mercy Clin Pediat Neurol, Springfield, MO USA Boston Childrens Hosp, Div Genet & Gen, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USAChao, Katherine R.论文数: 0 引用数: 0 h-index: 0机构: Broad Inst MIT & Harvard, Ctr Mendelian Genom, Boston, MA USA Boston Childrens Hosp, Div Genet & Gen, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USAFoley, A. Reghan论文数: 0 引用数: 0 h-index: 0机构: NIH, Neuromuscular & Neurogenet Disorders Childhood, Bldg 10, Bethesda, MD 20892 USA Boston Childrens Hosp, Div Genet & Gen, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USASchoots, Mirthe H.论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Univ Med Ctr Groningen, Dept Pathol, Groningen, Netherlands Boston Childrens Hosp, Div Genet & Gen, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USAJongbloed, Jan D. H.论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands Boston Childrens Hosp, Div Genet & Gen, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USABonnemann, Carsten G.论文数: 0 引用数: 0 h-index: 0机构: NIH, Neuromuscular & Neurogenet Disorders Childhood, Bldg 10, Bethesda, MD 20892 USA Boston Childrens Hosp, Div Genet & Gen, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USAAgrawal, Pankaj B.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Genet & Gen, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USA Boston Childrens Hosp, Manton Ctr Orphan Dis Res, 300 Longwood Ave, Boston, MA 02115 USA Harvard Med Sch, 300 Longwood Ave, Boston, MA 02115 USA Boston Childrens Hosp, Div Genet & Gen, Div Newborn Med, 300 Longwood Ave, Boston, MA 02115 USA
- [5] Genotype-phenotype correlationsARRHYTHMOGENIC RV CARDIOMYOPATHY/ DYSPLASIA: RECENT ADVANCES, 2007, : 21 - +Bauce, Barbara论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Cardiol Thorac & Vasc Sci, Padua, Italy Univ Padua, Dept Cardiol Thorac & Vasc Sci, Padua, ItalyNava, Andrea论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Cardiol Thorac & Vasc Sci, Padua, Italy Univ Padua, Dept Cardiol Thorac & Vasc Sci, Padua, Italy
- [6] Genotype-phenotype correlations in ACTA1 mutations that cause congenital myopathiesNEUROMUSCULAR DISORDERS, 2009, 19 (01) : 6 - 16Feng, Juan-Juan论文数: 0 引用数: 0 h-index: 0机构: Univ London Imperial Coll Sci Technol & Med, Natl Heart & Lung Inst, London SW3 6LY, England Univ London Imperial Coll Sci Technol & Med, Natl Heart & Lung Inst, London SW3 6LY, England论文数: 引用数: h-index:机构:
- [7] Exploring genotype-phenotype correlations in glutaric aciduria type 1JOURNAL OF INHERITED METABOLIC DISEASE, 2023, 46 (03) : 371 - 390Schuurmans, Imke M. E.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Dept Pediat, Med Ctr, Nijmegen, Netherlands Radboud Univ Nijmegen, Radboud Inst Mol Life Sci, Med Ctr, Nijmegen, Netherlands Radboud Univ Nijmegen, Amalia Childrens Hosp, Med Ctr, Nijmegen, Netherlands Univ Amsterdam, Emma Ctr Personalized Med, Dept Pediat & Human Genet, Med Ctr, Amsterdam, Netherlands Radboud Univ Nijmegen, Dept Pediat, Med Ctr, Nijmegen, NetherlandsDimitrov, Bianca论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Heidelberg, Ctr Child & Adolescent Med, Div Child Neurol & Metab Med, Heidelberg, Germany Radboud Univ Nijmegen, Dept Pediat, Med Ctr, Nijmegen, NetherlandsSchroter, Julian论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Heidelberg, Ctr Child & Adolescent Med, Div Child Neurol & Metab Med, Heidelberg, Germany Univ Hosp Heidelberg, Ctr Child & Adolescent Med, Div Pediat Epileptol, Heidelberg, Germany Radboud Univ Nijmegen, Dept Pediat, Med Ctr, Nijmegen, NetherlandsRibes, Antonia论文数: 0 引用数: 0 h-index: 0机构: Hosp Clin Barcelona, Dept Biochem & Mol Genet, Sect Inborn Errors Metab IBC, IDIBAPS,CIBERER, Barcelona, Spain Radboud Univ Nijmegen, Dept Pediat, Med Ctr, Nijmegen, Netherlandsde la Fuente, Ruben Perez论文数: 0 引用数: 0 h-index: 0机构: 12 Octubre Univ Hosp, Genet Dept, Madrid, Spain Radboud Univ Nijmegen, Dept Pediat, Med Ctr, Nijmegen, NetherlandsZamora, Berta论文数: 0 引用数: 0 h-index: 0机构: 12 Octubre Univ Hosp, Paediat Neuropsychol Dept, Madrid, Spain Radboud Univ Nijmegen, Dept Pediat, Med Ctr, Nijmegen, Netherlandsvan Karnebeek, Clara D. M.论文数: 0 引用数: 0 h-index: 0机构: Univ Amsterdam, Emma Ctr Personalized Med, Dept Pediat & Human Genet, Med Ctr, Amsterdam, Netherlands United Metab Dis, Delft, Netherlands Amsterdam Univ Med Ctr, Amsterdam Gastroenterol Endocrinol Metab, Amsterdam, Netherlands Radboud Univ Nijmegen, Dept Pediat, Med Ctr, Nijmegen, NetherlandsKolker, Stefan论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Heidelberg, Ctr Child & Adolescent Med, Div Child Neurol & Metab Med, Heidelberg, Germany Radboud Univ Nijmegen, Dept Pediat, Med Ctr, Nijmegen, NetherlandsGaranto, Alejandro论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Dept Pediat, Med Ctr, Nijmegen, Netherlands Radboud Univ Nijmegen, Radboud Inst Mol Life Sci, Med Ctr, Nijmegen, Netherlands Radboud Univ Nijmegen, Amalia Childrens Hosp, Med Ctr, Nijmegen, Netherlands Radboud Univ Nijmegen Med Ctr, Dept Human Genet, Nijmegen, Netherlands Radboud Univ Nijmegen, Dept Pediat, Med Ctr, Nijmegen, Netherlands
- [8] Genotype-phenotype correlations in retinoblastomaEUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 588 - 589Le Gall, Jessica论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Genet, Paris, France PSL Res Univ, Paris, France Inst Curie Hosp, Genet, Paris, FranceMahmoudi, Meriam论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Genet, Paris, France PSL Res Univ, Paris, France Inst Curie Hosp, Genet, Paris, FranceMezghani, Sarah论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Imaging, Paris, France Inst Curie Hosp, Genet, Paris, FranceBouchoucha, Yassine论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Pediat, Paris, France Inst Curie Hosp, Genet, Paris, FranceMatet, Alexandre论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Cite, Paris, France Inst Curie Hosp, Ocular Oncol, Paris, France Inst Curie Hosp, Genet, Paris, FranceCardoen, Liesbeth论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Imaging, Paris, France Inst Curie Hosp, Genet, Paris, FranceGhazelian, Hrant论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Genet, Paris, FranceCarriere, Jennifer论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Genet, Paris, France PSL Res Univ, Paris, France Inst Curie Hosp, Genet, Paris, FranceFort, Nicolas论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Genet, Paris, France PSL Res Univ, Paris, France Inst Curie Hosp, Genet, Paris, FranceGauthier-Villars, Marion论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Genet, Paris, France PSL Res Univ, Paris, France Inst Curie Hosp, Genet, Paris, FranceStoppa-Lyonnet, Dominique论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Genet, Paris, France Univ Paris Cite, Paris, France Inst Curie Hosp, Genet, Paris, FranceHua, Clement论文数: 0 引用数: 0 h-index: 0机构: PSL Res Univ, Paris, France Inst Curie Hosp, Mol Oncol Team, Paris, France Inst Curie Hosp, Genet, Paris, FranceRadvanyi, Francois论文数: 0 引用数: 0 h-index: 0机构: PSL Res Univ, Paris, France Inst Curie Hosp, Mol Oncol Team, Paris, France Inst Curie Hosp, Genet, Paris, FranceFreneaux, Paul论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Biopathol, Paris, France Inst Curie Hosp, Genet, Paris, FranceBrisse, Herve论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Imaging, Paris, France Inst Curie Hosp, Genet, Paris, FranceCassoux, Nathalie论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Cite, Paris, France Inst Curie Hosp, Ocular Oncol, Paris, France Inst Curie Hosp, Genet, Paris, FranceDoz, Francois论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Pediat, Paris, France Univ Paris Cite, Paris, France Inst Curie Hosp, Genet, Paris, FranceLisa, Golmard论文数: 0 引用数: 0 h-index: 0机构: Inst Curie Hosp, Genet, Paris, France PSL Res Univ, Paris, France Inst Curie Hosp, Genet, Paris, France
- [9] Genotype-phenotype correlations in FSHDBMC Medical Genomics, 12Nikolay Zernov论文数: 0 引用数: 0 h-index: 0机构: Research Center for Medical Genetics,School of BiomedicineMikhail Skoblov论文数: 0 引用数: 0 h-index: 0机构: Research Center for Medical Genetics,School of Biomedicine
- [10] GENOTYPE-PHENOTYPE CORRELATIONS IN PHENYLKETONURIACLINICA CHIMICA ACTA, 1993, 217 (01) : 15 - 21TREFZ, FK论文数: 0 引用数: 0 h-index: 0机构: UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANY UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANYBURGARD, P论文数: 0 引用数: 0 h-index: 0机构: UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANY UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANYKONIG, T论文数: 0 引用数: 0 h-index: 0机构: UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANY UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANYGOEBELSCHREINER, B论文数: 0 引用数: 0 h-index: 0机构: UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANY UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANYLICHTERKONECKI, U论文数: 0 引用数: 0 h-index: 0机构: UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANY UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANYKONECKI, D论文数: 0 引用数: 0 h-index: 0机构: UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANY UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANYSCHMIDT, E论文数: 0 引用数: 0 h-index: 0机构: UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANY UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANYSCHMIDT, H论文数: 0 引用数: 0 h-index: 0机构: UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANY UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANYBICKEL, H论文数: 0 引用数: 0 h-index: 0机构: UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANY UNIV HEIDELBERG,DEPT PEDIAT,W-6900 HEIDELBERG,GERMANY