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1 malformations include Kallmann syndrome and idiopathic hypogonadotropic hypogonadism.
2 thesized that mutations in genes involved in idiopathic hypogonadotropic hypogonadism, a congenital f
3 ond intracellular loop (IL2) of GPR54 causes idiopathic hypogonadotropic hypogonadism, a disorder cha
4 e identified prospectively among 50 men with idiopathic hypogonadotropic hypogonadism after a mean (+
5 ties in pubertal timing, including causes of idiopathic hypogonadotropic hypogonadism and Kallmann sy
9 tically heterogeneous disorder consisting of idiopathic hypogonadotropic hypogonadism (IHH) and anosm
14 the coding sequence of genes associated with idiopathic hypogonadotropic hypogonadism in 55 women wit
15 led receptor gene, cause autosomal recessive idiopathic hypogonadotropic hypogonadism in humans and m
16 cy in the human presents either as normosmic idiopathic hypogonadotropic hypogonadism (nIHH) or with
18 tion in GPR54, and an unrelated proband with idiopathic hypogonadotropic hypogonadism was determined
21 ith members who lacked pubertal development (idiopathic hypogonadotropic hypogonadism) was examined f
23 mutations in the GNRHR and GPR54 genes cause idiopathic hypogonadotropic hypogonadism with normal olf
24 ormone as compared with six patients who had idiopathic hypogonadotropic hypogonadism without GPR54 m
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