Associated Papers
Clinical genome sequencing in patients with hereditary breast and ovarian cancer: Concept, implementation and benefits.
Witt D et al.
Breast (edinburgh, Scotland), 2025
40403485 (PubMed )
Supplement: mmc2.xlsx › Actionable_findings
Evolutionary origin of germline pathogenic variants in human DNA mismatch repair genes.
Lei H et al.
Human Genomics, 2024
38287404 (PubMed )
Supplement: 40246_2024_573_MOESM3_ESM.xls › MLH1
Prevalence and Genotype-Phenotype Correlation of Lynch Syndrome in a Selected High-Risk Cohort from Qatar's Population.
Sidenna M et al.
Genes, 2022
36421850 (PubMed )
Supplement: genes-13-02176-s001.zip › Table_S1.pdf
Novel homozygous mutations in PATL2 lead to female infertility with oocyte maturation arrest.
Liu Z et al.
Journal of Assisted Reproduction and Genetics, 2020
Molecular approach to genetic and epigenetic pathogenesis of early-onset colorectal cancer.
Tezcan G et al.
World Journal of Gastrointestinal Oncology, 2016
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