(Q57729078)

English

Impact of 226C>T MSH2 gene mutation on cancer phenotypes in two HNPCC-associated highly-consanguineous families from Kuwait: emphasis on premarital genetic testing

article

In more languages

Statements

scholarly article

0 references

Impact of 226C>T MSH2 gene mutation on cancer phenotypes in two HNPCC-associated highly-consanguineous families from Kuwait: emphasis on premarital genetic testing (English)

0 references

1 reference

based on heuristic

inferred from title

object named as

Fahd Al-Mulla

6

0 references

author name string

Makia J. Marafie

1

0 references

Sadiqa Al-Awadi

2

0 references

Fatemah Al-Mosawi

3

0 references

Alaa Elshafey

4

0 references

Waleed Al-Ali

5

0 references

publication date

8 August 2009

0 references

Familial Cancer

0 references

8

0 references

4

0 references

289-298

0 references

https://scigraph.springernature.com/pub.10.1007/s10689-009-9275-3

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic clinics in arab communities: meeting individual, family and community needs.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role for genetic anticipation in Lynch syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Consanguinity among the Kuwaiti population

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial T-cell non-Hodgkin lymphoma caused by biallelic MSH2 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Management of extracolonic tumours in patients with Lynch syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Standards of care in diagnosis and testing for hereditary colon cancer.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

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

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal recessive disorders among Arabs: an overview from Kuwait

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of HNPCC: mutations of MMR genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Consanguineous marriages and their effects on common adult diseases: studies from an endogamous population

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without hematological malignancy and brain tumor.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biallelic germline mutations of mismatch-repair genes: a possible cause for multiple pediatric malignancies

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotype comparison of MLH1 and MSH2 mutation carriers in a cohort of 1,914 individuals undergoing clinical genetic testing in the United States.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Colorectal cancer in HNPCC: cumulative lifetime incidence, survival and tumour distribution. A report of 121 families with proven mutations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic susceptibility to non-polyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anticipation in lynch syndrome: still waiting for the answer

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extracolonic cancer in hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novelMSH2 germline mutation in homozygous state in two brothers with colorectal cancers diagnosed at the age of 11 and 12 years

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: Meeting Highlights and Bethesda Guidelines

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biallelic PMS2 mutations and a distinctive childhood cancer syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

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

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risk associated with germline DNA mismatch repair gene mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour

1 reference

https://pubmed.ncbi.nlm.nih.gov/19669601

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10689-009-9275-3

0 references

PubMed publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q57729078&oldid=1403875257"