Prevalence and phenotypes of APC and MUTYH mutations in patients with multiple colorectal adenomas. - Wikidata - wikimedia - TriplyDB

Prevalence and phenotypes of APC and MUTYH mutations in patients with multiple colorectal adenomas.

Prevalence and phenotypes of APC and MUTYH mutations in patients with multiple colorectal adenomas.

http://www.wikidata.org/entity/Q37163661

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Therapy-associated polyposis as a late sequela of cancer treatment.Novel mutations and phenotypic associations identified through APC, MUTYH, NTHL1, POLD1, POLE gene analysis in Indian Familial Adenomatous Polyposis cohort Genetic predisposition to colorectal cancer: where we stand and future perspectives Common colorectal cancer risk alleles contribute to the multiple colorectal adenoma phenotype, but do not influence colonic polyposis in FAP.Familial risk-colorectal cancer: ESMO Clinical Practice Guidelines.Familial colorectal cancer, beyond Lynch syndrome Genomic era diagnosis and management of hereditary and sporadic colon cancer.The genetic basis of familial adenomatous polyposis and its implications for clinical practice and risk management.Increased risk for colorectal adenomas and cancer in mono-allelic MUTYH mutation carriers: results from a cohort of North-African Jews.Germline TP53 Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family Registry A case series of intestinal adenomatous polyposis of unidentified etiology; a late effect of irradiation?Diagnostic Approach to Hereditary Colorectal Cancer Syndromes.Deep sequencing with intronic capture enables identification of an APC exon 10 inversion in a patient with polyposis.Adenoma development in familial adenomatous polyposis and MUTYH-associated polyposis: somatic landscape and driver genes.Racial variation in frequency and phenotypes of APC and MUTYH mutations in 6,169 individuals undergoing genetic testing Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis 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.Prevalence of germline PTEN, BMPR1A, SMAD4, STK11, and ENG mutations in patients with moderate-load colorectal polyps.Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer.Hereditary colorectal cancer syndromes and genetic testing.A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.Colorectal cancer in young adults.Hereditary and common familial colorectal cancer: evidence for colorectal screening.Familial colorectal cancer.A proposed staging system and stage-specific interventions for familial adenomatous polyposis Dispelling misconceptions in the management of familial adenomatous polyposis.Type and frequency of MUTYH variants in Italian patients with suspected MAP: a retrospective multicenter study.Clinical Characteristics of Multiple Colorectal Adenoma Patients Without Germline APC or MYH Mutations.Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases.Pseudoexons provide a mechanism for allele-specific expression of APC in familial adenomatous polyposis.ACMG technical standards and guidelines for genetic testing for inherited colorectal cancer (Lynch syndrome, familial adenomatous polyposis, and MYH-associated polyposis).Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis.Germline Genetic Features of Young Individuals with Colorectal Cancer.NTHL1 and MUTYH polyposis syndromes: two sides of the same coin?Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas.Germline mutations in patients with multiple colorectal polyps in China.Colorectal polyposis and inherited colorectal cancer syndromes.Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.The American Society of Colon and Rectal Surgeons Clinical Practice Guidelines for the Management of Inherited Polyposis Syndromes.

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P2860

Prevalence and phenotypes of APC and MUTYH mutations in patients with multiple colorectal adenomas.

http://www.wikidata.org/entity/Q37163661

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Prevalence and phenotypes of A ...... multiple colorectal adenomas.

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Prevalence and phenotypes of A ...... multiple colorectal adenomas.

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Prevalence and phenotypes of A ...... multiple colorectal adenomas.

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Prevalence and phenotypes of A ...... multiple colorectal adenomas.

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Prevalence and phenotypes of A ...... multiple colorectal adenomas.

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Prevalence and phenotypes of A ...... multiple colorectal adenomas.

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Prevalence and phenotypes of A ...... multiple colorectal adenomas.

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Akriti Dewanwala

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E Francis Cook

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Fay Kastrinos

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Lynn Anne Burbidge

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Richard J Wenstrup

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Shilpa Grover

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P2860

Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH

Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C-->T:A mutations

Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH

American College of Gastroenterology guidelines for colorectal cancer screening 2009 [corrected]

Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer

Germline susceptibility to colorectal cancer due to base-excision repair gene defects.

High frequency of MYH gene mutations in a subset of patients with familial adenomatous polyposis

MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps

Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk

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