Lv1
60 积分 2024-12-10 加入
Molecular Cloning of NELIN, a Putative Human Cytoskeleton Regulation Gene
2个月前
已关闭
Novel mutations in PMFBP1, TSGA10 and SUN5: Expanding the spectrum of mutations that may cause acephalic spermatozoa
4个月前
已关闭
Biallelic mutations in PMFBP1 cause acephalic spermatozoa
4个月前
已完结
Genetic mutation analysis of 22 patients with congenital absence of vas deferens: a single-center study
4个月前
已完结
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome
4个月前
已完结
A dominant negative FGFR1 mutation identified in a Kallmann syndrome patient
4个月前
已完结
Targeted next generation sequencing approach identifies eighteen new candidate genes in normosmic hypogonadotropic hypogonadism and Kallmann syndrome
4个月前
已完结
Screening candidate genes for mutations in patients with hypogonadotropic hypogonadism using custom genome resequencing microarrays
4个月前
已完结
Defective signaling through plexin-A1 compromises the development of the peripheral olfactory system and neuroendocrine reproductive axis in mice
4个月前
已完结
Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism
4个月前
已完结
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