GREM 1 and POLE variants in hereditary colorectal cancer syndromes-Reference-Cited by-同舟云学术

GREM 1 and POLE variants in hereditary colorectal cancer syndromes

Published:2015-10-23 Issue:1 Volume:55 Page:95-106
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosomes Cancer

Author:

Rohlin Anna¹²,Eiengård Frida¹²,Lundstam Ulf³,Zagoras Theofanis¹²,Nilsson Staffan⁴,Edsjö Anders²⁵,Pedersen Jan⁶,Svensson Janhenry⁷,Skullman Stefan⁷,Karlsson B. Göran⁸,Björk Jan⁹,Nordling Margareta¹²

Affiliation:

1. Department of Medical and Clinical GeneticsInstitute of Biomedicine, Sahlgrenska Academy at University of GothenburgGothenburg Sweden

2. Department of Clinical Pathology and GeneticsSahlgrenska University HospitalGothenburg Sweden

3. Department of SurgerySahlgrenska Academy at University of Gothenburg, Sahlgrenska University Hospital/ÖstraGothenburg Sweden

4. Mathematical Sciences, Chalmers University of TechnologyGothenburg Sweden

5. Department of PathologyInstitute of Biomedicine, Sahlgrenska Academy at University of GothenburgGothenburg Sweden

6. Department of Medical GeneticsRikshospitalet, University HospitalOslo Norway

7. Department of SurgerySkaraborg HospitalSkövde Sweden

8. The Swedish NMR‐Centre at University of GothenburgGothenburg Sweden

9. Department of MedicineThe Swedish Polyposis Registry, Karolinska InstituteStockholm Sweden

Publisher

Wiley

Subject

Cancer Research,Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/gcc.22314

Reference50 articles.

1. Explaining the Familial Colorectal Cancer Risk Associated with Mismatch Repair (MMR)-Deficient and MMR-Stable Tumors

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4. Control-free calling of copy number alterations in deep-sequencing data using GC-content normalization

5. ESEfinder: a web resource to identify exonic splicing enhancers

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