Cifuentes, Laura  |  Investigador

documento

• Absence of the CHEK2 c.1100delC mutation in familial breast and ovarian cancer in Colombia: a case-control study
• Absence of the CHEK2 c.1100delC mutation in familial breast and ovarian cancer in Colombia: a case-control study [version 1; peer review: 2 approved with reservations]
• BRCA1 and BRCA2 mutations in a sample of breast and ovarian cancer families from the Colombian pacific
• BRCA1 and BRCA2 mutations in breast and ovarian cancer families from south west Colombia
• Mutational analysis of BRCA1 and BRCA2 genes in women with familial breast cancer from different regions of Colombia
• Mutational analysis of BRCA1 and BRCA2 genes in women with familial breast cancer from different regions of Colombia
• Mutations of the CHEK2 gene in patients with cancer and their presence in the Latin American population
• Mutations of the CHEK2 gene in patients with cancer and their presence in the Latin American population [version 1; referees: awaiting peer review]
• Oral manifestations in patients with coronavirus disease 2019 (COVID-19) identified using text mining: an observational study
• Oral manifestations in patients with coronavirus disease 2019 (COVID-19) identified using text mining: an observational study
• Polimorfismos en genes de baja penetrancia como marcadores genéticos de riesgo de cáncer de mama familiar entre mujeres colombianas
• Polymorphisms of Low Penetrance Genes as Genetic Markers of Risk of Familial Breast Cancer among Colombian Wom
• Presence of periodontal pathogenic bacteria in blood of patients with coronary artery disease
• Presence of periodontal pathogenic bacteria in blood of patients with coronary artery disease
• Sequencing technology status of BRCA1/2 testing in Latin American Countries
• Sequencing technology status of BRCA1/2 testing in Latin American Countries
• Sequencing technology status of BRCA1/2 testing in Latin American Countries
• Sequencing technology status of BRCA1/2 testing in Latin American Countries
• Supplementary Material for: Mutations of the CHEK2 gene in patients with cancer and their presence in the Latin American population
• Supplementary Material for: Mutations of the CHEK2 gene in patients with cancer and their presence in the Latin American population
• Synchronous and multiple renal cell carcinoma, clear cell and papillary: An approach to clinically significant genetic abnormalities
• Synchronous and multiple renal cell carcinoma, clear cell and papillary: An approach to clinically significant genetic abnormalities.