Associated Papers
Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes.
Wonkam A et al.
Communications Biology, 2022
Genotypic and phenotypic spectrum of CCDC141 variants in a Chinese cohort with congenital hypogonadotropic hypogonadism.
Hou Q et al.
European Journal of Endocrinology, 2020
Clonal architectures and driver mutations in metastatic melanomas.
Ding L et al.
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25393105 (PubMed )
Supplement: pone.0111153.s002.zip › File_S2 › Table_S11.xls › Supp_Table_11
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