...
机译:部分隐性IFN-γR1缺乏症:来自11个亲属的14例患者的遗传,免疫学和临床特征
Department of Immunology,;
Laboratory of Human Genetics of Infectious Diseases, Necker Faculty, INSERM U980, Necker Medical School, University Paris Descartes, Paris, France,|St Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, USA,;
Department of Biochemistry, Molecular Biology, Physiology, Genetics and Immunology,;
Laboratory of Human Genetics of Infectious Diseases, Necker Faculty, INSERM U980, Necker Medical School, University Paris Descartes, Paris, France,;
Department of Clinical Sciences-Pharmacology Unit, Molecular and Translational Endocrinology Group and;
Laboratory of Human Genetics of Infectious Diseases, Necker Faculty, INSERM U980, Necker Medical School, University Paris Descartes, Paris, France,;
Department of Immunology,|Canarian Institute for Cancer Research, La Laguna, Santa Cruz de Tenerife, Spain,;
La;
机译:部分隐性IFN-γR1缺乏症:来自11个亲属的14例患者的遗传,免疫学和临床特征。
机译:遗传性IL-12p40缺陷:来自30种人的49例患者的遗传,免疫学和临床特征
机译:遗传性IL-12p40缺乏症:来自30个家庭的49位患者的遗传,免疫学和临床特征
机译:常染色体隐性高胆固醇血症:遗传学和临床方面
机译:炎症性肠病患者缺铁性贫血管理中的临床结果
机译:部分隐性IFN-γR1缺乏症:来自11个亲属的14例患者的遗传免疫学和临床特征
机译:部分隐性IFN-γR1缺乏症:来自11个亲属的14例患者的遗传,免疫学和临床特征