Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures (Q62978214)

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English	Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures	article

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instance of

scholarly article

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stated in

Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

title

Long term follow-up of HNPCC gene mutation carriers: compliance with screening and satisfaction with counseling and screening procedures (English)

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stated in

Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

main subject

Lynch syndrome

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based on heuristic

inferred from title

author

Hans Vasen

series ordinal

6

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stated in

Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

author name string

Anja Wagner

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

Ingrid van Kessel

series ordinal

2

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stated in

Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

Mieke G Kriege

series ordinal

3

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stated in

Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

Carli M J Tops

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

Juul Th Wijnen

series ordinal

5

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stated in

Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

Conny A van der Meer

series ordinal

7

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Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

Iris I H van Oostrom

series ordinal

8

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stated in

Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

Hanne Meijers-Heijboer

series ordinal

9

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stated in

Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

publication date

1 January 2005

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Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

published in

Familial Cancer

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stated in

Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

volume

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

issue

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

page(s)

295-300

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stated in

Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

cites work

Germ-line mutation of the hMSH6/GTBP gene in an atypical hereditary nonpolyposis colorectal cancer kindred

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16341806

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

American Society of Clinical Oncology Policy Statement Update: Genetic Testing for Cancer Susceptibility

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16341806

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychological and behavioral implications of abnormal mammograms

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16341806

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The outcome of endometrial carcinoma surveillance by ultrasound scan in women at risk of hereditary nonpolyposis colorectal carcinoma and familial colorectal carcinoma

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16341806

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Personal theories of inheritance, coping strategies, risk perception and engagement in hereditary non-polyposis colon cancer families offered genetic testing

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16341806

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16341806

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16341806

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comprehension of cancer risk one and 12 months after predictive genetic testing for hereditary non-polyposis colorectal cancer

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16341806

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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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16341806

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Colon cancer screening

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16341806

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16341806

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No Support for Endoscopic Surveillance for Gastric Cancer in Hereditary Non-Polyposis Colorectal Cancer

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16341806

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Colon cancer screening practices after genetic counseling and testing for hereditary nonpolyposis colorectal cancer

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16341806

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16341806

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risk associated with germline DNA mismatch repair gene mutations

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16341806

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risk in mutation carriers of DNA-mismatch-repair genes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16341806

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16341806

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S10689-005-0658-9

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

Dimensions Publication ID

1019202692

0 references

PubMed publication ID

16341806

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16341806

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16341806%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 January 2020

 

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