Mutation

Looking for VUS to Confirm Dominant Wolfram-like Syndrome Instead of Recessive Wolfram Syndrome

Natural History Study of Inherited Retinal Diseases

Integrative Sequencing In Germline and Hereditary Tumours

Liquid Biopsy Evaluation and Repository Development at Princess Margaret

Natural History Study of Patients with HPDL Mutations

Investigation of Tumour Spectrum of Germline Mutations in Breast and Ovarian Cancer Genes.

Neoadjuvant Umbrella Trial for Patients With Unresectable Stage III NSCLC Harboring Rare Mutations.

Investigating the Role of Genetics in Disease Predisposition

BioMEL- Diagnostic and Prognostic Factors in Melanoma.

Everolimus With Investigator's Choice of Chemotherapy in Advanced Triple-Negative Breast Cancer (TNBC) With Luminal Androgen Receptor (LAR) Subtype

Impact of COVID-19 SARS-CoV-2 Variability in ICU Hospitalized Patients With Severe Disease

Sotorasib in Advanced KRASG12C-mutated Non-small Cell Lung Cancer Patients With Comorbidities

C677T Methylenetetrahydrofolate Reductase Mutation

Molecular Profiling in Prostate Cancer

Utilizing Free DNA in Embryo Culture for PGT

Monitoring Alectinib Treatment by Detection of ALK Translocations in Serial Blood Samples From Non-Small Cell Lung Cancer Patients

Screening of Pulmonary Veino Occlusive Disease in Heterozygous EIF2AK4 Mutation Carriers

New Strategies of Genetic Study of Patients With Oculocutaneous Albinism

Clinical Value of Next Generation Sequencing in Endocrine Therapy for Advanced Hormone Receptor Positive/HER-2 Negative Breast Cancer

Utility of Plasma Circulating Tumor DNA (ctDNA) in Asymptomatic Subjects for the Detection of Neoplastic Disease