Development of esophageal squamous cell cancer in patients with FAMMM syndrome: Two clinical reports-Reference-Cited by-同舟云学术

Development of esophageal squamous cell cancer in patients with FAMMM syndrome: Two clinical reports

Published:2020-03 Issue:3 Volume:63 Page:103840
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

van der Wilk Berend J.,Noordman Bo J.,Atmodimedjo Peggy N.,Dinjens Winand N.M.,Laheij Robert J.F.,Wagner Anja,Wijnhoven Bas P.L.,van Lanschot J. Jan B.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference24 articles.

1. Aberrant p16 methylation, a possible epigenetic risk factor in familial esophageal squamous cell carcinoma;Abbaszadegan;Int. J. Gastrointest. Cancer,2005

2. CDKN2A germline mutations in familial pancreatic cancer;Bartsch;Ann. Surg.,2002

3. Systemic cancer and the FAMMM syndrome;Bergman;Br. J. Canc.,1990

4. High frequency of multiple melanomas and breast and pancreas carcinomas in CDKN2A mutation-positive melanoma families;Borg;J. Natl. Cancer Inst.,2000

5. Diagnostic detection of allelic losses and imbalances by next-generation sequencing: 1p/19q Co-deletion analysis of gliomas;Dubbink;J. Mol. Diagn.,2016

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