Double mutation of APC and BRCA1 in an Italian family

Author:

Vietri Maria Teresa,D'Elia Giovanna,Caliendo Gemma,Casamassimi Amelia,Resse Marianna,Passariello Luana,Cioffi Michele,Molinari Anna Maria

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference21 articles.

1. Hereditary diffuse gastric cancer and lynch syndromes in a BRCA1/2 negative breast cancer patient;Njoroge;Breast Cancer Res Treat,2017

2. Novel mutations and phenotypic associations identified through APC, MUTYH, NTHL1, POLD1, POLE gene analysis in Indian Familial Adenomatous Polyposis cohort;Khan;Sci Rep,2017

3. Familial Adenomatous polyposis syndrome: an update and review of extraintestinal manifestations;Dinarvand;Arch Pathol Lab Med,2019

4. A novel frameshift mutation in exon 12 of the adenomatous polyposis coli gene in an Italian family with familial adenomatous polyposis and desmoid tumour;Vietri;J Mol Genet Med,2010

5. Prevalence and phenotypes of APC and MUTYH mutations in patients with multiple colorectal adenomas;Grover;JAMA,2012

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