RCMI Coordinating Center (RCMI CC) Header Logo

Search Result Details

This page shows the details of why an item matched the keywords from your search.
One or more keywords matched the following items that are connected to Dutil, Julie
Item TypeName
Grant Defining breast cancer risk: the role of genetic variations in DNA repair genes
Academic Article Single-nucleotide polymorphisms in the lysyl oxidase-like protein 4 and complement component 3 genes are associated with increased risk for endometriosis and endometriosis-associated infertility.
Academic Article Identification of the prevalent BRCA1 and BRCA2 mutations in the female population of Puerto Rico.
Academic Article Genetic polymorphisms in RAD23B and XPC modulate DNA repair capacity and breast cancer risk in Puerto Rican women.
Academic Article The spectrum of BRCA1 and BRCA2 alleles in Latin America and the Caribbean: a clinical perspective.
Academic Article No Evidence for the Pathogenicity of the BRCA2 c.6937?+?594T>G Deep Intronic Variant: A Case-Control Analysis.
Academic Article Genetic Epidemiology of Breast Cancer in Latin America.
Academic Article An Interactive Resource to Probe Genetic Diversity and Estimated Ancestry in Cancer Cell Lines.
Academic Article Germline variants in cancer genes in high-risk non-BRCA patients from Puerto Rico.
Academic Article Complete and overlapping congenics proving the existence of a quantitative trait locus for blood pressure on Dahl rat chromosome 17.
Concept Genetic Predisposition to Disease
Academic Article BRCA1/2 mutations and risk-reducing bilateral salpingo-oophorectomy among Latinas: The UPTAKE study.
Academic Article Piloting a Spanish-Language Web-Based Tool for Hereditary Cancer Genetic Testing.
Search Criteria
  • Genetic Predisposition to Disease
RCMI CC is supported by the National Institute on Minority Health and Health Disparities, National Institutes of Health (NIH), through Grant Number U24MD015970. The contents of this site are solely the responsibility of the authors and do not necessarily represent the official views of the NIH

For technical support please contact support