Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families - Wikidata - awgldk - TriplyDB

Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families

Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families

http://www.wikidata.org/entity/Q35363025

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Duodenal adenoma surveillance in patients with familial adenomatous polyposis MUTYH the base excision repair gene family member associated with colorectal cancer polyposis Risk factors predicting desmoid occurrence in patients with familial adenomatous polyposis: a meta-analysis Mutational spectrum of APC and genotype-phenotype correlations in Greek FAP patients.Identification of 5 novel germline APC mutations and characterization of clinical phenotypes in Japanese patients with classical and attenuated familial adenomatous polyposis.Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects.Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families.Wireless capsule endoscopy in detecting small-intestinal polyps in familial adenomatous polyposis.Adenomatous polyposis coli in an elderly female nigerian Genetic testing for hereditary colorectal cancer.The differential diagnosis and surveillance of hereditary gastrointestinal polyposis syndromes.Desmoid tumours: our experience of six cases and review of literature.When is molecular genetic testing for colorectal cancer indicated?Genomic era diagnosis and management of hereditary and sporadic colon cancer.Optimal therapy for desmoid tumors: current options and challenges for the future.Mesenteric desmoid tumor of the interposed jejunal pouch after total gastrectomy.Genetic testing for polyposis: practical and ethical aspects.Large intron 14 rearrangement in APC results in splice defect and attenuated FAP.Molecular genetics of supernumerary tooth formation.Mutation Analysis of the APC Gene in a Chinese FAP Pedigree with Unusual Phenotype.Duodenal cancer in patients with familial adenomatous polyposis (FAP): results of a 10 year prospective study Evidence for genetic predisposition to desmoid tumours in familial adenomatous polyposis independent of the germline APC mutation.Prevention and management of duodenal polyps in familial adenomatous polyposis.High-resolution melting (HRM) re-analysis of a polyposis patients cohort reveals previously undetected heterozygous and mosaic APC gene mutations.Desmoid tumors complicating Familial Adenomatous Polyposis: a meta-analysis mutation spectrum of affected individuals Long-term outcome of sporadic and FAP-associated desmoid tumors treated with high-dose selective estrogen receptor modulators and sulindac: a single-center long-term observational study in 134 patients.Mutation cluster region, association between germline and somatic mutations and genotype-phenotype correlation in upper gastrointestinal familial adenomatous polyposis.A complex rearrangement in the APC gene uncovered by multiplex ligation-dependent probe amplification Hereditary Colorectal Cancer: Genetics and Screening Familial adenomatous polyposis: challenges and pitfalls of surgical treatment.Correlation between mutations and mRNA expression of APC and MUTYH genes: new insight into hereditary colorectal polyposis predisposition.The genetic basis of colonic adenomatous polyposis syndromes ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary Mutational spectrum of the APC and MUTYH genes and genotype-phenotype correlations in Brazilian FAP, AFAP, and MAP patients.Genotype-phenotype correlations in 19 Dutch cases with APC gene deletions and a literature review.Clinicopathological features of familial adenomatous polyposis in Korean patients.Desmoid tumors in the pediatric population Diagnosis, surveillance, and treatment strategies for familial adenomatous polyposis: rationale and update.Thyroid cancer complicating familial adenomatous polyposis: mutation spectrum of at-risk individuals.

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Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families

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Can APC mutation analysis cont ...... perience from 680 FAP families

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Can APC mutation analysis cont ...... perience from 680 FAP families

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Can APC mutation analysis cont ...... perience from 680 FAP families

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Caspari R

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Fahnenstich J

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Friedl W

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Jungck M

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Lamberti C

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Möslein G

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Propping P

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Genotype-phenotype correlations in attenuated adenomatous polyposis coli.

Mutation and cancer: statistical study of retinoblastoma

A simple salting out procedure for extracting DNA from human nucleated cells

beta-catenin signaling and cancer

Identification of FAP locus genes from chromosome 5q21

Identification and characterization of the familial adenomatous polyposis coli gene

Variable phenotype of familial adenomatous polyposis in pedigrees with 3' mutation in the APC gene.

Management of duodenal adenomas in 98 patients with familial adenomatous polyposis.

Novel germline APC gene mutation in a large familial adenomatous polyposis kindred displaying variable phenotypes.

Notable intrafamilial phenotypic variability in a kindred with familial adenomatous polyposis and an APC mutation in exon 9.

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