换一批The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome.
第一作者：
Samuel D,Quaynor
第一单位：
Section of Reproductive Endocrinology, Infertility, and Genetics, Department of Obstetrics and Gynecology, Institute of Molecular Medicine and Genetics, Neuroscience Program, Georgia Health Sciences University, Augusta, Georgia 30912, USA.
作者：
医学主题词
青少年(Adolescent);成年人(Adult);女(雌)性(Female);基因频率(Gene Frequency);人类(Humans);性腺功能减退症(Hypogonadism);卡尔曼综合征(Kallmann Syndrome);男(雄)性(Male);模型, 生物学(Models, Biological);突变(Mutation);多态性, 单核苷酸(Polymorphism, Single Nucleotide);患病率(Prevalence);青年人(Young Adult)
DOI
10.1016/j.fertnstert.2011.09.046
PMID
22035731
发布时间
2022-04-19
- 浏览12
Fertility and sterility
1424-1430.e6页
相似文献
- 中文期刊
- 外文期刊
- 学位论文
- 会议论文
