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Patients with rare cancers in the Drug Rediscovery Protocol (DRUP) benefit from genomics-guided treatment
High-Mannose N-Glycans as Malignant Progression Markers in Early-Stage Colorectal Cancer
Specific (sialyl-)Lewis core 2 O-glycans differentiate colorectal cancer from healthy colon epithelium
Prevalence of mismatch repair deficiency and Lynch syndrome in a cohort of unselected small bowel adenocarcinomas
Statin use is associated with a reduced incidence of colorectal cancer expressing SMAD4
The coding microsatellite mutation profile of PMS2-deficient colorectal cancer
Yield and costs of molecular diagnostics on thyroid cytology slides in the Netherlands, adapting the Bethesda classification
IGF2 is a potential factor in RAI-refractory differentiated thyroid cancer
The diverse molecular profiles of lynch syndrome-associated colorectal cancers are (highly) dependent on underlying germline mismatch repair mutations
Mismatch repair deficiency is rare in bone and soft tissue tumors
Targeting EML4-ALK gene fusion variant 3 in thyroid cancer
Use of sanger and next-generation sequencing to screen for mosaic and intronic APC variants in unexplained colorectal polyposis patients
N-glycomic signature of stage II colorectal cancer and its association with the tumor microenvironment
Recurrent APC splice variant c.835-8A > G in patients with unexplained colorectal polyposis fulfilling the colibactin mutational signature
Digenic inheritance of MSH6 and MUTYH variants in familial colorectal cancer
Transanal minimally invasive surgery (TAMIS) versus endoscopic submucosal dissection (ESD) for resection of non-pedunculated rectal lesions (TRIASSIC study): study protocol of a European multicenter randomised controlled trial
Metabolic reprogramming related to whole-chromosome instability in models for Hurthle cell carcinoma
The missing heritability of familial colorectal cancer
Attenuated isolated 3 ' signal
The complexity of screening PMS2 in DNA isolated from formalin-fixed paraffin-embedded material
Declining detection rates for APC and biallelic MUTYH variants in polyposis patients, implications for DNA testing policy
A unique case of two somatic APC mutations in an early onset cribriform-morular variant of papillary thyroid carcinoma and overview of the literature
Unmet therapeutic, educational and scientific needs in parathyroid disorders: Consensus Statement from the first European Society of Endocrinology Workshop (PARAT)
Targeted treatment options of recurrent radioactive iodine refractory Hürthle cell cancer
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