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International Journal of Cancer|January 18, 2018
Rare missense mutations in RECQL and POLG associate with inherited predisposition to breast cancerAnna Tervasmäki, Tuomo Mantere, Jaana M Hartikainen, et al.
Scientific Reports|May 28, 2021
Genetic contributions to the expression of acquired causes of cardiac hypertrophy in non-ischemic sudden cardiac death victimsLauri Holmström, Katri Pylkäs, Anna Tervasmäki, et al.
Plos Genetics|August 14, 2023
Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibilityTimo A Kumpula, Sandra Vorimo, Taneli T Mattila, et al.
International Journal of Cancer|August 21, 2016
FANCM c.5101C>T mutation associates with breast cancer survival and treatment outcomeJohanna I Kiiski, Rainer Fagerholm, Anna Tervasmäki, et al.
Breast Cancer Research and Treatment|July 14, 2017
FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish populationJohanna I Kiiski, Anna Tervasmäki, Liisa M Pelttari, et al.
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