Works matching IS 13899600 AND DT 2005 AND VI 4
Results: 69
Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures.
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- Familial Cancer, 2005, v. 4, n. 4, p. 295, doi. 10.1007/s10689-005-0658-9
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MLH1 and MSH2 Mutations in Colombian Families with Hereditary Nonpolyposis Colorectal Cancer (Lynch syndrome) – Description of Four Novel Mutations.
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- Familial Cancer, 2005, v. 4, n. 4, p. 285, doi. 10.1007/s10689-005-4523-7
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BAP1 and Breast Cancer Risk.
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- Familial Cancer, 2005, v. 4, n. 4, p. 273, doi. 10.1007/s10689-005-2833-4
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Linkage of a Pedigree Drawing Program and Database to a Program for Determining BRCA Mutation Carrier Probability.
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- Familial Cancer, 2005, v. 4, n. 4, p. 313, doi. 10.1007/s10689-005-8849-y
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Key word Index Volume 4.
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- Familial Cancer, 2005, v. 4, n. 4, p. 337, doi. 10.1007/s10689-005-4695-1
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- Article
Neurofibromatosis 2 (NF2) and Malignant Mesothelioma in a Man with a Constitutional NF2 Missense Mutation.
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- Familial Cancer, 2005, v. 4, n. 4, p. 321, doi. 10.1007/s10689-005-0659-8
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Mutational analysis of hMsh6 in Israeli HNPCC and HNPCC-like Families.
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- Familial Cancer, 2005, v. 4, n. 4, p. 291, doi. 10.1007/s10689-005-1255-7
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Survival of Patients with Ovarian Cancer due to a Mismatch Repair Defect.
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- Familial Cancer, 2005, v. 4, n. 4, p. 301, doi. 10.1007/s10689-005-6573-2
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Patient Satisfaction of BRCA1/2 Genetic Testing by Women at High Risk for Breast Cancer Participating in a Prevention Trial.
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- Familial Cancer, 2005, v. 4, n. 4, p. 279, doi. 10.1007/s10689-005-1474-y
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Contents Volume 4.
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- Familial Cancer, 2005, v. 4, n. 4, p. 339, doi. 10.1007/s10689-005-4696-0
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- Article
Acknowledgements.
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- Familial Cancer, 2005, v. 4, n. 4, p. 335, doi. 10.1007/s10689-005-4694-2
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- Article
Behavioral and Economic Impact of a Familial History of Cancers.
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- Familial Cancer, 2005, v. 4, n. 4, p. 307, doi. 10.1007/s10689-005-3143-6
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Syndrome of Early Onset Colon Cancers, Hematologic Malignancies & Features of Neurofibromatosis in HNPCC Families with Homozygous Mismatch Repair Gene Mutations.
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- Familial Cancer, 2005, v. 4, n. 4, p. 323, doi. 10.1007/s10689-005-8351-6
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Lack of Germ-line Mutations at the Specific BRCA1-IRIS Coding Sequence in 114 Spanish High-risk Breast/ovarian Families.
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- Familial Cancer, 2005, v. 4, n. 4, p. 317, doi. 10.1007/s10689-005-1236-x
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The Incidence of Lynch Syndrome.
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- Familial Cancer, 2005, v. 4, n. 3, p. 233
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Clinical Description of the Lynch Syndrome [Hereditary Nonpolyposis Colorectal Cancer (HNPCC)].
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- Familial Cancer, 2005, v. 4, n. 3, p. 219, doi. 10.1007/s10689-004-3906-5
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- Article
Gynecologic Cancers in Lynch Syndrome/HNPCC.
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- Familial Cancer, 2005, v. 4, n. 3, p. 249, doi. 10.1007/s10689-005-1838-3
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Lynch Syndrome Genes.
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- Familial Cancer, 2005, v. 4, n. 3, p. 227
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Use of Microsatellite Instability and Immunohistochemistry Testing for the Identification of Individuals at Risk for Lynch Syndrome.
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- Familial Cancer, 2005, v. 4, n. 3, p. 255, doi. 10.1007/s10689-004-1447-6
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Surveillance in Lynch Syndrome.
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- Familial Cancer, 2005, v. 4, n. 3, p. 267, doi. 10.1007/s10689-005-1475-x
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Introduction.
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- Familial Cancer, 2005, v. 4, n. 3, p. 209, doi. 10.1007/s10689-004-2526-4
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Evolution of the Nomenclature for the Hereditary Colorectal Cancer Syndromes.
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- Familial Cancer, 2005, v. 4, n. 3, p. 211, doi. 10.1007/s10689-004-4489-x
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The Tumor Spectrum in the Lynch Syndrome.
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- Familial Cancer, 2005, v. 4, n. 3, p. 245, doi. 10.1007/s10689-004-7994-z
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Guest editorial.
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- Familial Cancer, 2005, v. 4, n. 3, p. 207, doi. 10.1007/s10689-005-8658-3
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Frequency of Familial Colon Cancer and Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome) in a Large Population Database.
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- Familial Cancer, 2005, v. 4, n. 3, p. 239, doi. 10.1007/s10689-005-0657-x
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Informing one’s family about genetic testing for hereditary non-polyposis colorectal cancer (HNPCC): a retrospective exploratory study.
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- Familial Cancer, 2005, v. 4, n. 2, p. 163, doi. 10.1007/s10689-004-7992-1
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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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Abstracts of the 1st Conference of InSiGHT, the International Society for Gastrointestinal Hereditary Tumors, Newcastle upon Tyne, United Kingdom, 14-17 June 2005.
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- Familial Cancer, 2005, v. 4, p. 25, doi. 10.1007/s10689-005-4150-3
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Poster Presentations.
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- Familial Cancer, 2005, v. 4, p. 63
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Free Paper Session 7.
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- Familial Cancer, 2005, v. 4, p. 57
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Free Paper Session 6.
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- Familial Cancer, 2005, v. 4, p. 55
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Free Paper Session 5.
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- Familial Cancer, 2005, v. 4, p. 52
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