An Individual with Both MUTYH-Associated Polyposis and Lynch Syndrome Identified by Multi-Gene Hereditary Cancer Panel Testing: A Case Report.

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An Individual with Both MUTYH-Associated Polyposis and Lynch Syndrome Identified by Multi-Gene Hereditary Cancer Panel Testing: A Case Report.

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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An Individual with Both MUTYH- ...... Panel Testing: A Case Report.

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An Individual with Both MUTYH- ...... Panel Testing: A Case Report.

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An Individual with Both MUTYH- ...... Panel Testing: A Case Report.

@en

An Individual with Both MUTYH- ...... Panel Testing: A Case Report.

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An Individual with Both MUTYH- ...... Panel Testing: A Case Report.

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An Individual with Both MUTYH- ...... Panel Testing: A Case Report.

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P1476

An Individual with Both MUTYH- ...... Panel Testing: A Case Report.

@en

P2093

Christopher A Tan

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Ryan Bisson

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Stephanie A Cohen

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P2860

The genetic basis of Lynch syndrome and its implications for clinical practice and risk management.

Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer.

Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene.

ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes

Germline truncating mutations in both MSH2 and BRCA2 in a single kindred.

Feasibility of screening for Lynch syndrome among patients with colorectal cancer.

High Prevalence of Hereditary Cancer Syndromes in Adolescents and Young Adults With Colorectal Cancer

Characterization of mutant MUTYH proteins associated with familial colorectal cancer.

A case of endometrial cancer in the context of a BRCA2 mutation and double heterozygosity for Lynch syndrome.

Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines.

P304

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scholarly article

P356

10.3389/FGENE.2016.00036

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P478

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P577

2016-03-16T00:00:00Z

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P698

27014339

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4792865

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