Centro de investigación
Fundación Pública Galega de Medicina Xenómica
Publicacións (4) Publicacións nas que participase algún/ha investigador/a
2022
-
Author Correction: Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease (Nature Communications, (2020), 11, 1, (995), 10.1038/s41467-019-14275-y)
Nature Communications
-
Erratum: Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk (European journal of human genetics : EJHG (2022) 30 3 (349-362))
European journal of human genetics : EJHG
-
Erratum: Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants (Genetics in Medicine (2022) 24(1) (119–129), (S1098360021011308), (10.1016/j.gim.2021.08.016))
Genetics in Medicine
-
Hairy patches as early dermatological signs of Gorlin syndrome in a patient with a novel PTCH1 genetic variant
Journal of Dermatology