Associated Papers
Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism.
Kotan LD et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
Tumor genetic heterogeneity analysis of chronic sun-damaged melanoma.
Sanna A et al.
Pigment Cell & Melanoma Research, 2020
31811783 (PubMed )
Supplement: PCMR-33-480-s003.xls › Supplementary_Table_3
Select a paper to view details