Dilemmas in the management of screen-detected lesions in patients at high risk for pancreatic cancer.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 111, doi. 10.1007/s10689-016-9915-3
- By:
- Publication type:
- Article
Works matching IS 13899600 AND DT 2017 AND VI 16 AND IP 1
Results: 20
1
2
Characterization of BRCA1 and BRCA2 variants found in a Norwegian breast or ovarian cancer cohort.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 1, doi. 10.1007/s10689-016-9916-2
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- Publication type:
- Article
3
First description of mutational analysis of MLH1, MSH2 and MSH6 in Algerian families with suspected Lynch syndrome.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 57, doi. 10.1007/s10689-016-9917-1
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- Publication type:
- Article
4
Community attitudes towards a Jewish community BRCA1/2 testing program.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 17, doi. 10.1007/s10689-016-9918-0
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- Publication type:
- Article
5
Frequency of germline PALB2 mutations among women with epithelial ovarian cancer.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 29, doi. 10.1007/s10689-016-9919-z
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- Publication type:
- Article
6
Do women change their breast cancer mammogram screening behaviour after BRCA1/2 testing?
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 35, doi. 10.1007/s10689-016-9920-6
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- Publication type:
- Article
7
BRCA testing within the Department of Veterans Affairs: concordance with clinical practice guidelines.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 41, doi. 10.1007/s10689-016-9921-5
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- Publication type:
- Article
8
Hereditary leiomyomatosis and renal cell cancer syndrome: identification and clinical characterization of a novel mutation in the FH gene in a Colombian family.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 117, doi. 10.1007/s10689-016-9922-4
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- Publication type:
- Article
9
Calculating the optimal surveillance for head and neck paraganglioma in SDHB-mutation carriers.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 123, doi. 10.1007/s10689-016-9923-3
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- Publication type:
- Article
10
Nevoid basal cell carcinoma syndrome caused by splicing mutations in the PTCH1 gene.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 131, doi. 10.1007/s10689-016-9924-2
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- Publication type:
- Article
11
Mutational analysis of TP53 gene in Tunisian familial hematological malignancies and sporadic acute leukemia cases.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 153, doi. 10.1007/s10689-016-9931-3
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- Publication type:
- Article
12
Association of monoallelic MUTYH mutation among Egyptian patients with colorectal cancer.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 83, doi. 10.1007/s10689-016-9927-z
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- Publication type:
- Article
13
Genetically diagnosed Birt-Hogg-Dubé syndrome and familial cerebral cavernous malformations in the same individual: a case report.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 139, doi. 10.1007/s10689-016-9928-y
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- Publication type:
- Article
14
Hereditary breast and ovarian cancer: successful systematic implementation of a group approach to genetic counselling.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 51, doi. 10.1007/s10689-016-9929-x
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- Publication type:
- Article
15
A novel germline POLE mutation causes an early onset cancer prone syndrome mimicking constitutional mismatch repair deficiency.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 67, doi. 10.1007/s10689-016-9925-1
- By:
- Publication type:
- Article
16
Performance of Lynch syndrome predictive models in quantifying the likelihood of germline mutations in patients with abnormal MLH1 immunoexpression.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 73, doi. 10.1007/s10689-016-9926-0
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- Publication type:
- Article
17
Pancreas-sparing total duodenectomy for Spigelman stage IV duodenal polyposis associated with familial adenomatous polyposis: experience of 10 cases at a single institution.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 91, doi. 10.1007/s10689-016-9932-2
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- Publication type:
- Article
18
Factors associated with cancer worries in individuals participating in annual pancreatic cancer surveillance.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 143, doi. 10.1007/s10689-016-9930-4
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- Publication type:
- Article
19
Exploring clinicians' attitudes about using aspirin for risk reduction in people with Lynch Syndrome with no personal diagnosis of colorectal cancer.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 99, doi. 10.1007/s10689-016-9933-1
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- Publication type:
- Article
20
Multi-gene panel testing for hereditary cancer susceptibility in a rural Familial Cancer Program.
- Published in:
- Familial Cancer, 2017, v. 16, n. 1, p. 159, doi. 10.1007/s10689-016-9913-5
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- Publication type:
- Article