Natruly FeliuBadaló

Alvaro Monteiro

MUTATIONS IN HUMAN GENETIC DISEASE - volume 1

Natalia Feliubadaló on Behance

Discovery and implications of polygenicity of common diseases

Variants of uncertain clinical significance in hereditary breast and ovarian cancer genes: best practices in functional analysis for clinical annotation

Impact of proactive high-throughput functional assay data on BRCA1 variant interpretation in 3684 patients with breast or ovarian cancer

Amanda E Toland, PhD Ohio State cancer researcher

Catalogo-navidad-2017-feliubadalo

Cancers, Free Full-Text

Frontiers The emergence of Fanconi anaemia type S: a phenotypic spectrum of biallelic BRCA1 mutations

Structural basis for substrate specificity of heteromeric transporters of neutral amino acids

IJMS, Free Full-Text

Mayonnaises / dressings

Frontiers The emergence of Fanconi anaemia type S: a phenotypic spectrum of biallelic BRCA1 mutations

PDF) A Collaborative Effort to Define Classification Criteria for ATM Variants in Hereditary Cancer Patients