Late onset asymptomatic pancreatic neuroendocrine tumor – A case report on the phenotypic expansion for MEN1-Reference-Cited by-同舟云学术

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Late onset asymptomatic pancreatic neuroendocrine tumor – A case report on the phenotypic expansion for MEN1

Published:2017-07-21 Issue:1 Volume:15 Page:
ISSN:1897-4287
Container-title:Hereditary Cancer in Clinical Practice
language:en
Short-container-title:Hered Cancer Clin Pract

Author:

Kaiwar Charu,Macklin Sarah K.,Gass Jennifer M.,Jackson Jessica,Klee Eric W.,Hines Stephanie L.,Stauffer John A.,Atwal Paldeep S.^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Oncology

Link

http://link.springer.com/content/pdf/10.1186/s13053-017-0070-0.pdf

Reference15 articles.

1. Chandrasekharappa SC, et al. Positional cloning of the gene for multiple endocrine neoplasia-type 1. Science. 1997;276(5311):404–7.

2. Knudson AG. Hereditary cancer: two hits revisited. J Cancer Res Clin. Oncologia. 1996;122(3):135–40.

3. Pannett AA, Thakker RV. Somatic mutations in MEN type 1 tumors, consistent with the Knudson “two-hit” hypothesis. J Clin Endocrinol Metab. 2001;86(9):4371–4.

4. Marini F, et al. Multiple endocrine neoplasia type 1. Orphanet J Rare Dis. 2006;1:38.

5. Lemos MC, Thakker RV. Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene. Hum Mutat. 2008;29(1):22–32.

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