Molecular analysis of theAPCandMYHgenes in Czech families affected by FAP or multiple adenomas: 13 novel mutations
Author:
Funder
Ministry of Education, Youth and Sports, Czech Republic
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.9224/fullpdf
Cited by 27 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Germline mutations of the adenomatous polyposis coli (APC) gene in Algerian familial adenomatous polyposis cohort: first report;Molecular Biology Reports;2022-02-10
2. Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the APC gene in patients with familial adenomatous polyposis (FAP);Journal of Clinical Laboratory Analysis;2021-03-26
3. APC Splicing Mutations Leading to In-Frame Exon 12 or Exon 13 Skipping Are Rare Events in FAP Pathogenesis and Define the Clinical Outcome;Genes;2021-02-28
4. Pathogenic APC Variants in Latvian Familial Adenomatous Polyposis Patients;Medicina;2019-09-20
5. Molecular basis of familial adenomatous polyposis in the southeast of Brazil: identification of six novel mutations;The International Journal of Biological Markers;2019-03
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