The Molecular Basis of Inherited Reproductive Disorders
收藏DataCite Commons2022-11-16 更新2024-07-13 收录
下载链接：
https://dash.nichd.nih.gov/study/228877
下载链接
链接失效反馈官方服务：
资源简介：
The aims of this study are: 1) to identify genes that play a role in human pubertal development and reproduction, 2) to characterize the phenotypic spectrum of patients with these gene defects, and 3) to discern the mode of inheritance for disorders caused by these gene defects. We are specifically interested in genes that cause Kallmann syndrome, idiopathic hypogonadotropic hypogonadism (IHH), precocious (early) puberty, and delayed puberty.
提供机构：
NICHD Data and Specimen Hub
创建时间：
2022-11-15
