Prevalence of PALB2 mutation c.509_510delGA in unselected breast cancer patients from Central and Eastern Europe.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 137, doi. 10.1007/s10689-013-9684-1
- By:
- Publication type:
- Article
Works matching IS 13899600 AND DT 2014 AND VI 13 AND IP 2
Results: 23
1
2
Evaluation after five years of the cancer genetic counselling programme of Valencian Community (Eastern Spain).
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 301, doi. 10.1007/s10689-013-9693-0
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- Publication type:
- Article
3
Deletion of exons 1-3 of the MEN1 gene in a large Italian family causes the loss of menin expression.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 273, doi. 10.1007/s10689-014-9702-y
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- Publication type:
- Article
4
Barrett's esophagus in the patients with familial adenomatous polyposis.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 213, doi. 10.1007/s10689-013-9638-7
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- Publication type:
- Article
5
Is intraductal tubulopapillary neoplasia a new entity in the spectrum of familial pancreatic cancer syndrome?
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 227, doi. 10.1007/s10689-013-9696-x
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- Publication type:
- Article
6
Prophylactic total gastrectomy in hereditary diffuse gastric cancer: identification of two novel CDH1 gene mutations-a clinical observational study.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 231, doi. 10.1007/s10689-013-9698-8
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- Publication type:
- Article
7
Misperceptions of ovarian cancer risk in women at increased risk for hereditary ovarian cancer.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 153, doi. 10.1007/s10689-013-9687-y
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- Publication type:
- Article
8
Baseline and post prophylactic tubal-ovarian surgery CA125 levels in BRCA1 and BRCA2 mutation carriers.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 197, doi. 10.1007/s10689-013-9697-9
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- Publication type:
- Article
9
Providing patient education: impact on quantity and quality of family health history collection.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 325, doi. 10.1007/s10689-014-9701-z
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- Publication type:
- Article
10
The MUTYH hotspot mutations p.G396D and p.Y179C do not cause substantial genetic susceptibility to biliary cancer.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 243, doi. 10.1007/s10689-014-9699-2
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- Publication type:
- Article
11
Ectopic Cushing syndrome associated with thymic carcinoid tumor as the first presentation of MEN1 syndrome-report of a family with MEN1 gene mutation.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 267, doi. 10.1007/s10689-013-9692-1
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- Publication type:
- Article
12
Inversion of exons 1-7 of the MSH2 gene is a frequent cause of unexplained Lynch syndrome in one local population.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 219, doi. 10.1007/s10689-013-9688-x
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- Publication type:
- Article
13
Large genomic rearrangement of BRCA1 and BRCA2 genes in familial breast cancer patients in Korea.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 205, doi. 10.1007/s10689-014-9704-9
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- Publication type:
- Article
14
Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 257, doi. 10.1007/s10689-013-9639-6
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- Publication type:
- Article
15
RAD51 135G>C and TP53 Arg72Pro polymorphisms and susceptibility to breast cancer in Serbian women.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 173, doi. 10.1007/s10689-013-9690-3
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- Publication type:
- Article
16
Impact of familial risk and mammography screening on prognostic indicators of breast disease among women from the Ontario site of the Breast Cancer Family Registry.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 163, doi. 10.1007/s10689-013-9689-9
- By:
- Publication type:
- Article
17
A randomized controlled trial of diet and physical activity in BRCA mutation carriers.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 181, doi. 10.1007/s10689-013-9691-2
- By:
- Publication type:
- Article
18
Potential genetic anticipation in hereditary leiomyomatosis-renal cell cancer (HLRCC).
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 281, doi. 10.1007/s10689-014-9703-x
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- Publication type:
- Article
19
Breast cancer risk assessment in 8,824 women attending a family history evaluation and screening programme.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 189, doi. 10.1007/s10689-013-9694-z
- By:
- Publication type:
- Article
20
More breast cancer patients prefer BRCA-mutation testing without prior face-to-face genetic counseling.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 143, doi. 10.1007/s10689-013-9686-z
- By:
- Publication type:
- Article
21
Capsule endoscopy versus magnetic resonance enterography for the detection of small bowel polyps in Peutz-Jeghers syndrome.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 249, doi. 10.1007/s10689-014-9700-0
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- Publication type:
- Article
22
Attitudes and knowledge of medical practitioners to hereditary cancer clinics and cancer genetic testing.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 311, doi. 10.1007/s10689-013-9695-y
- By:
- Publication type:
- Article
23
Comparison of attitudes regarding preimplantation genetic diagnosis among patients with hereditary cancer syndromes.
- Published in:
- Familial Cancer, 2014, v. 13, n. 2, p. 291, doi. 10.1007/s10689-013-9685-0
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- Publication type:
- Article