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Paper Details

Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility.
PLoS Genet
0
2023
13, 31 kb deletion, CNVs, Copy number variants, HSD17B14, HSD17B14 deletion, RAD51C, RAD52, RAD52 delins, alleles, breast cancer, copy number variants, genes, hereditary breast cancer, hereditary disease, retrotransposon, single nucleotide variants
Author NameAffiliation
Outi KuisminMedical Research Center Oulu and PEDEGO Research Unit, Oulu University Hospital and University of Oulu
Jukka S MoilanenMedical Research Center Oulu and PEDEGO Research Unit, Oulu University Hospital and University of Oulu
Christian GilissenDepartment of Human Genetics and Radboud Institute of Medical Life Sciences, Radboud University Medical Center
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