Works matching IS 13899600 AND DT 2007 AND VI 6 AND IP 1
Results: 20
Utility of computed tomographic colonography in surveillance for hereditary nonpolyposis colorectal cancer syndrome.
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- Familial Cancer, 2007, v. 6, n. 1, p. 135, doi. 10.1007/s10689-007-9116-1
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- Article
Molecular diagnosis of neurofibromatosis type 1: 2 years experience.
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- Familial Cancer, 2007, v. 6, n. 1, p. 21, doi. 10.1007/s10689-006-9001-3
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The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome.
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- Familial Cancer, 2007, v. 6, n. 1, p. 1, doi. 10.1007/s10689-006-0014-8
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- Article
Risks of cancer due to a single BRCA1 mutation in an extended Utah kindred.
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- Familial Cancer, 2007, v. 6, n. 1, p. 63, doi. 10.1007/s10689-006-9106-8
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- Article
Familial colorectal cancer referral to regional genetics department—a single centre experience.
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- Familial Cancer, 2007, v. 6, n. 1, p. 81, doi. 10.1007/s10689-006-9108-6
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- Article
Family history is neglected in the work-up of patients with colorectal cancer: a quality assessment using cancer registry data.
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- Familial Cancer, 2007, v. 6, n. 1, p. 131
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- Article
Heterozygote BRCA1 status and skewed chromosome X inactivation.
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- Familial Cancer, 2007, v. 6, n. 1, p. 153, doi. 10.1007/s10689-006-9102-z
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A case of Muir-Torre syndrome associated with mucinous hepatic cholangiocarcinoma and a novel germline mutation of the MSH2 gene.
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- Familial Cancer, 2007, v. 6, n. 1, p. 141, doi. 10.1007/s10689-006-9105-9
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The interval between cancer diagnosis among mothers and offspring in a population-based cohort.
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- Familial Cancer, 2007, v. 6, n. 1, p. 121
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Improved survival in BRCA2 carriers with ovarian cancer.
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- Familial Cancer, 2007, v. 6, n. 1, p. 113
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The management of families affected by hereditary non-polyposis colorectal cancer (HNPCC).
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- Familial Cancer, 2007, v. 6, n. 1, p. 13, doi. 10.1007/s10689-006-9000-4
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Occurrence of both breast and ovarian cancer in a woman is a marker for the BRCA gene mutations: a population-based study from Western Sweden.
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- Familial Cancer, 2007, v. 6, n. 1, p. 35, doi. 10.1007/s10689-006-9101-0
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- Article
Very high incidence of familial colorectal cancer in Newfoundland: a comparison with Ontario and 13 other population-based studies.
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- Familial Cancer, 2007, v. 6, n. 1, p. 53, doi. 10.1007/s10689-006-9104-x
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- Article
Identification of a founder BRCA2 mutation in Sardinian breast cancer families.
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- Familial Cancer, 2007, v. 6, n. 1, p. 73, doi. 10.1007/s10689-006-9107-7
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- Article
An association between the 4G polymorphism in the PAI-1 promoter and the development of aggressive fibromatosis (desmoid tumor) in familial adenomatous polyposis patients.
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- Familial Cancer, 2007, v. 6, n. 1, p. 89, doi. 10.1007/s10689-006-9109-5
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- Article
Gastric carcinoid: germline and somatic mutation of the neurofibromatosis type 1 gene.
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- Familial Cancer, 2007, v. 6, n. 1, p. 147, doi. 10.1007/s10689-006-9002-2
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- Article
The natural history of a combined defect in MSH6 and MUTYH in a HNPCC family.
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- Familial Cancer, 2007, v. 6, n. 1, p. 43, doi. 10.1007/s10689-006-9103-y
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- Article
A missense germline mutation in exon 7 of the MSH2 gene in a HNPCC family from center-Italy.
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- Familial Cancer, 2007, v. 6, n. 1, p. 97
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Acceptance of preventive surgeries by Israeli women who had undergone BRCA testing.
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- Familial Cancer, 2007, v. 6, n. 1, p. 159, doi. 10.1007/s10689-006-0013-9
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Study comparing two types of screening provision for people with von Hippel-Lindau disease.
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- Familial Cancer, 2007, v. 6, n. 1, p. 103, doi. 10.1007/s10689-006-9111-y
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- Article