(Q54469117)

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Polyposis and early cancer in a patient with low penetrant mutations in MSH6 and APC: hereditary colorectal cancer as a polygenic trait.

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Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

Polyposis and early cancer in a patient with low penetrant mutations in MSH6 and APC: hereditary colorectal cancer as a polygenic trait. (English)

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Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

colorectal cancer

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based on heuristic

inferred from title

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based on heuristic

inferred from title

2

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Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

Finn Cilius Nielsen

9

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Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

10

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Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

Ole Thorlacius-Ussing

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Ole Thorlacius-Ussing

4

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author name string

Henrik Okkels

1

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Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

Karen Lindorff-Larsen

3

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Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

Per Gandrup

5

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Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

Jan Lindebjerg

6

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Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

Peter Stubbeteglbjaerg

7

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Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

John R Oestergaard

8

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Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

publication date

9 March 2006

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Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

International Journal of Colorectal Disease

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Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

21

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Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

8

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

847-850

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Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

https://scigraph.springernature.com/pub.10.1007/s00384-006-0086-9

0 references

A double germline mutations in the APC and p53 genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16525781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gastrointestinal cancers and neurofibromatosis type 1 features in children with a germline homozygous MLH1 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16525781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

I1307K APC and hMLH1 mutations in a non-Jewish family with hereditary non-polyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16525781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Café-au-lait spots and early onset colorectal neoplasia: a variant of HNPCC?

1 reference

https://pubmed.ncbi.nlm.nih.gov/16525781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic approaches to identifying breast cancer susceptibility factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/16525781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lessons from hereditary colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16525781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

1 reference

https://pubmed.ncbi.nlm.nih.gov/16525781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapidly progressive adenomatous polyposis in a patient with germline mutations in both the APC and MLH1 genes: the worst of two worlds.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16525781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial endometrial cancer in female carriers of MSH6 germline mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16525781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16525781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16525781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Double frameshift mutations in APC and MSH2 in the same individual

1 reference

https://pubmed.ncbi.nlm.nih.gov/16525781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Insulin resistance syndrome in children

1 reference

https://pubmed.ncbi.nlm.nih.gov/16525781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers

1 reference

https://pubmed.ncbi.nlm.nih.gov/16525781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurofibromatosis von Recklinghausen type I phenotype and early onset of cancers in siblings compound heterozygous for mutations in MSH6

1 reference

https://pubmed.ncbi.nlm.nih.gov/16525781

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00384-006-0086-9

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 May 2018

http://europepmc.org/abstract/MED/16525781

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