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机译:由于新型纯合突变引起的GNRH受体贩运的缺乏导致三个Prepubertal兄弟姐妹的特发性低因素性腺病药
Cent S Univ Ctr Med Genet Sch Life Sci Changsha Hunan Peoples R China;
Cent S Univ Ctr Med Genet Sch Life Sci Changsha Hunan Peoples R China;
Cent S Univ Ctr Med Genet Sch Life Sci Changsha Hunan Peoples R China;
Cent S Univ Ctr Med Genet Sch Life Sci Changsha Hunan Peoples R China;
Cent S Univ Ctr Med Genet Sch Life Sci Changsha Hunan Peoples R China;
Cent S Univ Ctr Med Genet Sch Life Sci Changsha Hunan Peoples R China;
Cent S Univ Ctr Med Genet Sch Life Sci Changsha Hunan Peoples R China;
Hypogonadotropic hypogonadism; GNRHR; Whole exome sequencing; Prepubertal; Novel mutation; Genetic diagnosis;
机译:由于新型纯合突变引起的GNRH受体贩运的缺乏导致三个Prepubertal兄弟姐妹的特发性低因素性腺病药
机译:具有GnRH受体突变的正常性特发性促性腺激素减退症(综述)
机译:常规发作性低因素性腺性腺性腺低因素(审查)
机译:纯合蛋白C缺乏症:鉴定导致突变蛋白C分泌受损的新型错义突变
机译:由两个兄弟姐妹中的新型GNRH1变异引起的正常性性腺功能减退性腺功能减退
机译:特发性低血管增不基因的性腺性腺增生变异性:与促性腺激素释放激素受体1中纯合突变相关的自发逆转