Population carrier frequency of hMSH2 and hMLH1 mutations.
about
Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer.Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genesMetachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgeryContinuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients.Genetic testing strategies in newly diagnosed endometrial cancer patients aimed at reducing morbidity or mortality from lynch syndrome in the index case or her relativesDoes risk of endometrial cancer for women without a germline mutation in a DNA mismatch repair gene depend on family history of endometrial cancer or colorectal cancer?Chemoprevention in patients with genetic risk of colorectal cancersGuidance on gastrointestinal surveillance for hereditary non-polyposis colorectal cancer, familial adenomatous polypolis, juvenile polyposis, and Peutz-Jeghers syndrome.Prevalence of pathological germline mutations of hMLH1 and hMSH2 genes in colorectal cancer.Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers.Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study.Hereditary non-polyposis colon cancerDetermining the frequency of de novo germline mutations in DNA mismatch repair genes.Childhood cancers in families with and without Lynch syndrome.Aspirin, Ibuprofen, and the Risk of Colorectal Cancer in Lynch Syndrome.Risk of breast cancer in Lynch syndrome: a systematic review.Penetrance of colorectal cancer among MLH1/MSH2 carriers participating in the colorectal cancer familial registry in Ontario.Two cases of successful pregnancies after hysteroscopic removal of endometrioid adenocarcinoma grade I, stage IA, in young women with Lynch syndromeManagement of young onset colorectal cancer: divergent practice in the East of England.Criteria and prediction models for mismatch repair gene mutations: a review.An Overview of Autosomal Dominant Tumour Syndromes with Prominent Features in the Oral and Maxillofacial Region.Unstable DNA repair genes shaped by their own sequence modifying phenotypes.Multivitamin, calcium and folic acid supplements and the risk of colorectal cancer in Lynch syndrome.
P2860
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P2860
Population carrier frequency of hMSH2 and hMLH1 mutations.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
2000年论文
@zh
2000年论文
@zh-cn
name
Population carrier frequency of hMSH2 and hMLH1 mutations.
@ast
Population carrier frequency of hMSH2 and hMLH1 mutations.
@en
type
label
Population carrier frequency of hMSH2 and hMLH1 mutations.
@ast
Population carrier frequency of hMSH2 and hMLH1 mutations.
@en
prefLabel
Population carrier frequency of hMSH2 and hMLH1 mutations.
@ast
Population carrier frequency of hMSH2 and hMLH1 mutations.
@en
P2093
P356
P1476
Population carrier frequency of hMSH2 and hMLH1 mutations.
@en
P2093
A Carothers
G Petersen
L Aaltonen
M Porteous
S M Farrington
P2888
P304
P356
10.1054/BJOC.2000.1520
P407
P577
2000-12-01T00:00:00Z
P5875
P6179
1021820153