Pages that link to "Q54488788"

The following pages link to Etiology of familial breast cancer with undetected BRCA1 and BRCA2 mutations: clinical implications. (Q54488788):

Displaying 9 items.

• Prevalence of Germline Mutations in Genes Engaged in DNA Damage Repair by Homologous Recombination in Patients with Triple-Negative and Hereditary Non-Triple-Negative Breast Cancers (Q35665705) (← links)
• Genomic rearrangement screening of the BRCA1 from seventy Iranian high-risk breast cancer families. (Q37593704) (← links)
• A novel loss-of-function heterozygous BRCA2 c.8946_8947delAG mutation found in a Chinese woman with family history of breast cancer (Q47898378) (← links)
• BRCA1/2-negative hereditary triple-negative breast cancers exhibit BRCAness (Q48906011) (← links)
• The laminin-derived peptide C16 regulates GPNMB expression and function in breast cancer. (Q50433076) (← links)
• The cancer genome: from structure to function. (Q53087702) (← links)
• Identification of miR-10b, miR-26a, miR-146a and miR-153 as potential triple-negative breast cancer biomarkers. (Q54989577) (← links)
• Decreased CDK10 expression correlates with lymph node metastasis and predicts poor outcome in breast cancer patients - a short report. (Q55042390) (← links)
• BRCA1 c.68_69delAG (exon2), c.181T>G (exon5), c.798_799delTT and 943ins10 (exon11) mutations in Burkina Faso (Q56335931) (← links)