Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and Surveillance-Reference-Cited by-同舟云学术

Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and Surveillance

Published:2017-06 Issue:8 Volume:152 Page:1876-1880.e1
ISSN:0016-5085
Container-title:Gastroenterology
language:en
Short-container-title:Gastroenterology

Author:

Lieberman Sari,Walsh Tom,Schechter Menachem,Adar Tomer,Goldin Eran,Beeri Rachel,Sharon Nitzan,Baris Hagit,Ben Avi Liat,Half Elizabeth,Lerer Israela,Shirts Brian H.,Pritchard Colin C.,Tomlinson Ian,King Mary-Claire,Levy-Lahad Ephrat,Peretz Tamar,Goldberg Yael

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference17 articles.

1. Clinical and molecular features of the hereditary mixed polyposis syndrome

2. A Prospective Study of The Clinical, Genetic, Screening, and Pathologic Features of A Family With Hereditary Mixed Polyposis Syndrome

3. Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1

4. Defining the polyposis/colorectal cancer phenotype associated with the Ashkenazi GREM1 duplication: counselling and management recommendations

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