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Molecular tumor testing in patients with Lynch-like syndrome reveals a de novo mosaic variant of a mismatch repair gene transmitted to offspring.
Not available
S-EPMC7575584
|
biostudies-literature
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Early Colorectal Cancers Provide New Evidence for a Lynch Syndrome-to-CMMRD Phenotypic Continuum.
Not available
S-EPMC6721314
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biostudies-literature
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Diagnostic challenges in a child with early onset desmoplastic medulloblastoma and homozygous variants in MSH2 and MSH6.
Not available
S-EPMC5839041
|
biostudies-literature
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Cyclin D1 rare variants in UK multiple adenoma and early-onset colorectal cancer patients.
Not available
S-EPMC5140020
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biostudies-literature
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Role of rare variants in undetermined multiple adenomatous polyposis and early-onset colorectal cancer.
Not available
S-EPMC5140019
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biostudies-literature
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Lynch syndrome: influence of additional susceptibility variants on cancer risk.
Not available
S-EPMC10474080
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biostudies-literature
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AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer.
Not available
S-EPMC10107344
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biostudies-literature
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Glioma oncogenesis in the Constitutional mismatch repair deficiency (CMMRD) syndrome.
Not available
S-EPMC11372297
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biostudies-literature
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Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts.
Not available
S-EPMC3647358
|
biostudies-literature
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Stoma-free Survival After Rectal Cancer Resection With Anastomotic Leakage: Development and Validation of a Prediction Model in a Large International Cohort.
Not available
S-EPMC10549897
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biostudies-literature
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