V. Krutílková

Telomere length in peripheral blood cells of germline TP53 mutation carriers is shorter than that of normal individuals of corresponding age

M. Trková, Z. Sedlacek, D. Sumerauer, 2007, Cancer.

ISPD gene homozygous deletion identified by SNP array confirms prenatal manifestation of Walker-Warburg syndrome.

M. Trková, J. Horáček, V. Bečvářova, 2015, European journal of medical genetics.

[Genetic Syndromes Predisposing to Tumors of Central Nervous System in Children].

V. Krutílková, 2015, Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti.

Identification of five new families strengthens the link between childhood choroid plexus carcinoma and germline TP53 mutations.

M. Trková, Z. Sedlacek, R. Kodet, 2005, European journal of cancer.

[Li-Fraumeni syndrome].

K. Petráková, M. Pálácova, P. Plevova, 2009, Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti.

Recommendations for care of patients with breast and ovarian cancer and healthy individuals with germline mutations in BRCA1 or BRCA2 gene

K. Petráková, Z. Kleibl, E. Macháčková, 2003 .

[Gorlin syndrome].

P. Plevova, A. Puchmajerová, V. Krutílková, 2009, Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti.

ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

James M. Hodge, E. Burnside, Y. Kamatani, 2023, Clinical cancer research : an official journal of the American Association for Cancer Research.

[A dissecting aortic aneurysm in a female patient with Turner syndrome].

E. Seemanová, E. Koudelková, J. Chlumský, 2000, Vnitrni lekarstvi.