Works matching IS 13899600 AND DT 2005 AND VI 4 AND IP 2
Results: 20
Informing one’s family about genetic testing for hereditary non-polyposis colorectal cancer (HNPCC): a retrospective exploratory study.
- Published in:
- Familial Cancer, 2005, v. 4, n. 2, p. 163, doi. 10.1007/s10689-004-7992-1
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- Article
An unusual case of Turcot’s syndrome associated with ileal adenocarcinoma, intestinal non-Hodgkin’s lymphoma, and duodenal adenocarcinoma. Review of the classification and genetic basis of Turcot’s syndrome.
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- Familial Cancer, 2005, v. 4, n. 2, p. 139, doi. 10.1007/s10689-004-2759-2
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- Article
Genetic uptake in BRCA-mutation families is related to emotional and behavioral communication characteristics of index patients.
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- Familial Cancer, 2005, v. 4, n. 2, p. 115, doi. 10.1007/s10689-004-7991-2
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- Article
A comparison of the phenotype and genotype in adenomatous polyposis patients with and without a family history.
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- Familial Cancer, 2005, v. 4, n. 2, p. 127, doi. 10.1007/s10689-004-5814-0
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- Article
The BRCA1 exon 13 duplication in the Swedish population.
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- Familial Cancer, 2005, v. 4, n. 2, p. 191, doi. 10.1007/s10689-004-7023-2
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- Article
The CHEK2 1100delC allele is not relevant for risk assessment in HNPCC and HBCC Spanish families.
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- Familial Cancer, 2005, v. 4, n. 2, p. 183
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- Article
APC and β-catenin protein expression patterns in HNPCC-related endometrial and colorectal cancers.
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- Familial Cancer, 2005, v. 4, n. 2, p. 187, doi. 10.1007/s10689-004-6130-4
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- Article
Referrals of patients to colorectal cancer genetics services in south-east Scotland.
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- Familial Cancer, 2005, v. 4, n. 2, p. 151, doi. 10.1007/s10689-004-4488-y
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- Article
Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH.
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- Familial Cancer, 2005, v. 4, n. 2, p. 145, doi. 10.1007/s10689-004-6131-3
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- Article
The use of preventive measures among healthy women who carry a BRCA1 or BRCA2 mutation.
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- Familial Cancer, 2005, v. 4, n. 2, p. 97, doi. 10.1007/s10689-005-4215-3
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Measurement of psychological factors associated with genetic testing for hereditary breast, ovarian and colon cancers.
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- Familial Cancer, 2005, v. 4, n. 2, p. 195, doi. 10.1007/s10689-004-1446-7
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- Article
High prevalence of two BRCA1 mutations, 4154delA and 5382insC, in Latvia.
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- Familial Cancer, 2005, v. 4, n. 2, p. 77, doi. 10.1007/s10689-004-2758-3
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- Article
The TP53 mutational spectrum and frequency of CHEK2*1100delC in Li–Fraumeni-like kindreds.
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- Familial Cancer, 2005, v. 4, n. 2, p. 177, doi. 10.1007/s10689-004-1946-5
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- Article
Abdominal desmoid in familial adenomatous polyposis presenting as a pancreatic cystic lesion.
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- Familial Cancer, 2005, v. 4, n. 2, p. 135, doi. 10.1007/s10689-004-1923-z
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- Article
Ratio of male to female births in the offspring of BRCA1 and BRCA2 carriers.
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- Familial Cancer, 2005, v. 4, n. 2, p. 73, doi. 10.1007/s10689-004-2102-y
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- Article
Psychological distress in women at risk of hereditary breast/ovarian or HNPCC cancers in the absence of demonstrated mutations.
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- Familial Cancer, 2005, v. 4, n. 2, p. 121, doi. 10.1007/s10689-004-7995-y
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- Article
Predictors of participation in clinical and psychosocial follow-up of the kConFab breast cancer family cohort.
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- Familial Cancer, 2005, v. 4, n. 2, p. 105, doi. 10.1007/s10689-004-6129-x
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- Article
The Tyr978X BRCA1 mutation: occurrence in non-Jewish Iranians and haplotype in French-Canadian and non-Ashkenazi Jews.
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- Familial Cancer, 2005, v. 4, n. 2, p. 85, doi. 10.1007/s10689-004-2101-z
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- Article
SISE matters: the Sum of Information on Seventy-yr-old Equivalents measures pedigree information content when assessing the risk of HNPCC in a family.
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- Familial Cancer, 2005, v. 4, n. 2, p. 169, doi. 10.1007/s10689-004-7251-5
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- Article
A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques.
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- Familial Cancer, 2005, v. 4, n. 2, p. 89, doi. 10.1007/s10689-004-5812-2
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- Article