Associated Papers
Stepwise ABC system for classification of any type of genetic variant.
Houge G et al.
European Journal of Human Genetics : Ejhg, 2022
33981013 (PubMed )
Supplement: 41431_2021_903_MOESM2_ESM.xlsx › Ark1
Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome.
Xu N et al.
Fertility and Sterility, 2011
Identification of risk genes in Chinese nonobstructive azoospermia patients based on whole-exome sequencing.
Liu YJ et al.
Asian Journal of Andrology, 0
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