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Rheumatology International|October 24, 2009
Systemic lupus erythematosus as a first presentation of common variable immunodeficiency associated with infrequent mannose-binding lectin gene polymorphismsMaite Torres-Salido, Josefina Cortés-Hernández, Eva Balada, et al.Anales De Pediatria|November 21, 2025
Genetic counseling in pediatrics: Clinical implications and challenges in genomic medicineDiana Salinas Chaparro, Patricia Muñoz Cabello, Gema Escribano Serrano, et al.Breast (Edinburgh, Scotland)|March 16, 2025
Identifying germline pathogenic variants in breast cancer using tumor sequencingMara Cruellas, Andri Papakonstantinou, Adrià López-Fernández, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2021
Patients' and professionals' perspective of non-in-person visits in hereditary cancer: predictors and impact of the COVID-19 pandemicAdrià López-Fernández, Guillermo Villacampa, Elia Grau, et al.Journal of Genetic Counseling|February 7, 2023
Role of psychological background in cancer susceptibility genetic testing distress: It is not only about a positive resultAdrià López-Fernández, Guillermo Villacampa, Mònica Salinas, et al.Journal of Medical Genetics|November 29, 2022
Clinical and psychological implications of secondary and incidental findings in cancer susceptibility genes after exome sequencing in patients with rare disordersEstela Carrasco, Adrià López-Fernández, Marta Codina-Sola, et al.Journal of the National Cancer Institute|April 2, 2025
A randomized study of 2 risk assessment models for individualized breast cancer risk estimationAdrià López-Fernández, Laura Duran-Lozano, Guillermo Villacampa, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 28, 2025
The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS)Linda A J Hendricks, Katja C J Verbeek, Janneke H M Schuurs-Hoeijmakers, et al.Pageof 1