Novel Germline APC Mutations in Swedish Patients with Familial Adenomatous Polyposis and Gardner Syndrome
Author:
Publisher
Informa UK Limited
Subject
Gastroenterology
Link
http://www.tandfonline.com/doi/pdf/10.1080/003655200750056691
Reference20 articles.
1. Hepatoblastoma, pigmented ocular fundus lesions and jaw lesions in gardner syndrome
2. Alleles of the APC gene: An attenuated form of familial polyposis
3. Identification and characterization of the familial adenomatous polyposis coli gene
4. Binding of APC to the Human Homolog of the Drosophila Discs Large Tumor Suppressor Protein
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1. Rare Germline Variants in the Adenomatous Polyposis Coli Gene Associated with Dental and Osseous Anomalies;International Journal of Molecular Sciences;2024-07-26
2. The Benefits of CBCT Imaging in the Diagnosis of Individuals with Craniofacial Anomalies;Journal of the California Dental Association;2023-08-24
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. APC Germline Mutations in Individuals Being Evaluated for Familial Adenomatous Polyposis;The Journal of Molecular Diagnostics;2013-01
5. Inactivation of promoter 1B of APC causes partial gene silencing: evidence for a significant role of the promoter in regulation and causative of familial adenomatous polyposis;Oncogene;2011-06-06
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