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UnknownPrimary mucinous adenocarcinoma of the vermiform appendix with high grade microsatellite instability.
Not available
S-EPMC3119391 | biostudies-literature
UnknownTargeted deep-intronic sequencing in a cohort of unexplained cases of suspected Lynch syndrome.
Not available
S-EPMC7170855 | biostudies-literature
UnknownCombined loss of CDH1 and downstream regulatory sequences drive early-onset diffuse gastric cancer and increase penetrance of hereditary diffuse gastric cancer.
Not available
S-EPMC10361908 | biostudies-literature
UnknownGenotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes.
Not available
S-EPMC9810541 | biostudies-literature
UnknownClopidogrel and proton pump inhibitor (PPI) interaction: separate intake and a non-omeprazole PPI the solution?
Not available
S-EPMC3352012 | biostudies-literature
UnknownCritical assessment of secondary findings in genes linked to primary arrhythmia syndromes.
Not available
S-EPMC7187207 | biostudies-literature
UnknownExtending the critical regions for mutations in the non-coding gene RNU4ATAC in another patient with Roifman Syndrome.
Not available
S-EPMC6230649 | biostudies-literature
UnknownReclassification of VUS in <i>BRCA1</i> and <i>BRCA2</i> using the new <i>BRCA1</i>/<i>BRCA2</i> ENIGMA track set demonstrates the superiority of ClinGen ENIGMA Expert Panel specifications over the standard ACMG/AMP classification system.
Not available
S-EPMC11869971 | biostudies-literature
UnknownBiallelic MUTYH mutations can mimic Lynch syndrome.
Not available
S-EPMC4200426 | biostudies-literature
UnknownChorea-acanthocytosis genotype in the original critchley kentucky neuroacanthocytosis kindred.
Not available
S-EPMC4615612 | biostudies-literature
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