Paolo Radice
Istituto Nazionale dei Tumori
302 papers found
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Rare variants in XRCC2 as breast cancer susceptibility alleles: Table 1
UploadGermline mutations in BRIP1 and PALB2 in Jewish high cancer risk families
Download from link.springer.com11q13 is a Susceptibility Locus for Hormone Receptor Positive Breast Cancer†
Download from mediatum.ub.tum.deThe SNP rs895819 in miR-27a is not associated with familial breast cancer risk in Italians
UploadSequencing Analysis of SLX4/FANCP Gene in Italian Familial Breast Cancer Cases
Download from doi.org19p13.1 Is a Triple-Negative-Specific Breast Cancer Susceptibility Locus
Download from mediatum.ub.tum.deThe KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriers
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