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Paper Details

Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity.
Breast Cancer Res
7
2018
ATM, BRCA1, BRCA2, Breast cancer, CDKN2A, CHEK2, Fanconi, Fanconi pathway, Fanconi pathway genes, Fraumeni syndrome, Li, Li-, Li-Fraumeni syndrome, Li-Fraumeni(-like), Li-Fraumeni(-like) breast cancer, Li-Fraumeni(-like) syndrome, Li-Fraumeni-like, PALB2, RECQ family genes, RUNX1, TP53, TP53 gene, TP53 variants, breast cancer, cancer, cancer predisposition genes, candidate genes, coding regions, germline, hereditary breast cancer, noncoding regions, p14ARF, patients, single-nucleotide variants, tumor, women
Author NameAffiliation
Thomas IlligHannover Medical School
Doris SteinemannHannover Medical School
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Release 1.2