MLH1

Clinical and Genetic Characterization of Constitutional MLH1 Promoter Hypermethylation: Implications for Lynch Syndrome Diagnosis.

Syndrome de Lynch par hyperméthylation constitutionnelle du promoteur MLH1

The germline MLH1 c.2054 C>T mutation disrupts DNA mismatch repair and is detectable by digital PCR.

Syndrome de Lynch

Gene-specific cancer risks in female Lynch syndrome carriers: A copula-based meta-analysis

Syndrome de Lynch — risques cancéreux spécifiques par gène chez les femmes

Universal Tumor Screening in Colorectal Cancer: Role of MMR Immunohistochemistry for Lynch Syndrome and Early-Onset CRC.

Syndrome de Lynch — dépistage tumoral universel du cancer colorectal

Genetic Landscape of Lynch Syndrome in a High-Risk Serbian Cohort: Predominance of MLH1 Variants and Implications for Risk-Based Testing.

Syndrome de Lynch

Performance of PREMM5, clinical criteria, and immunohistochemistry for MMR proteins in genetic risk assessment of Mexican patients with colorectal cancer.

Syndrome de Lynch et prédisposition héréditaire au cancer colorectal

Mismatch Repair Deficiency in Upper Gastrointestinal and Pancreaticobiliary Cancers: Integrating Multimodal Molecular Data in Clinical Practice.

Syndrome de Lynch et cancers digestifs hauts

Real-world uptake of Lynch syndrome testing among patients with mismatch repair-deficient endometrial cancer in Québec

Syndrome de Lynch — cancer de l'endomètre