Desmoid tumors: clinical features and outcome of an unpredictable and challenging manifestation of familial adenomatous polyposis.
- Published in:
- Familial Cancer, 2015, v. 14, n. 2, p. 211, doi. 10.1007/s10689-014-9772-x
- By:
- Publication type:
- Article
Works matching IS 13899600 AND DT 2015 AND VI 14 AND IP 2
Results: 17
1
2
Health professionals' evaluation of delivering treatment-focused genetic testing to women newly diagnosed with breast cancer.
- Published in:
- Familial Cancer, 2015, v. 14, n. 2, p. 265, doi. 10.1007/s10689-014-9770-z
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- Publication type:
- Article
3
First-Line sunitinib in patients with renal cell carcinoma (RCC) in von Hippel-Lindau (VHL) disease: clinical outcome and patterns of radiological response.
- Published in:
- Familial Cancer, 2015, v. 14, n. 2, p. 309, doi. 10.1007/s10689-014-9771-y
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- Publication type:
- Article
4
Exome sequencing reveals three novel candidate predisposition genes for diffuse gastric cancer.
- Published in:
- Familial Cancer, 2015, v. 14, n. 2, p. 241, doi. 10.1007/s10689-015-9778-z
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- Publication type:
- Article
5
Comparison of proctocolectomy and ileal pouch-anal anastomosis to colectomy and ileorectal anastomosis in familial adenomatous polyposis.
- Published in:
- Familial Cancer, 2015, v. 14, n. 2, p. 221, doi. 10.1007/s10689-014-9773-9
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- Publication type:
- Article
6
The roles of AXIN2 in tumorigenesis and epigenetic regulation.
- Published in:
- Familial Cancer, 2015, v. 14, n. 2, p. 325, doi. 10.1007/s10689-014-9775-7
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- Publication type:
- Article
7
A risk of digestive tract neoplasms susceptibility in miR-146a and miR-196a2.
- Published in:
- Familial Cancer, 2015, v. 14, n. 2, p. 229, doi. 10.1007/s10689-014-9776-6
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- Publication type:
- Article
8
Impact of BRCA1/ 2 mutation on young women's 5-year parenthood rates: a prospective comparative study (GENEPSO-PS cohort).
- Published in:
- Familial Cancer, 2015, v. 14, n. 2, p. 273, doi. 10.1007/s10689-014-9777-5
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- Publication type:
- Article
9
Large genomic rearrangements in the familial breast and ovarian cancer gene BRCA1 are associated with an increased frequency of high risk features.
- Published in:
- Familial Cancer, 2015, v. 14, n. 2, p. 287, doi. 10.1007/s10689-015-9785-0
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- Publication type:
- Article
10
Parental age and Neurofibromatosis Type 1: a report from the NF1 Patient Registry Initiative.
- Published in:
- Familial Cancer, 2015, v. 14, n. 2, p. 317, doi. 10.1007/s10689-014-9774-8
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- Publication type:
- Article
11
The breast cancer immunophenotype of TP53-p.R337H carriers is different from that observed among other pathogenic TP53 mutation carriers.
- Published in:
- Familial Cancer, 2015, v. 14, n. 2, p. 333, doi. 10.1007/s10689-015-9779-y
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- Publication type:
- Article
12
The effect of oral 3,3′-diindolylmethane supplementation on the 2:16α-OHE ratio in BRCA1 mutation carriers.
- Published in:
- Familial Cancer, 2015, v. 14, n. 2, p. 281, doi. 10.1007/s10689-015-9783-2
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- Publication type:
- Article
13
High-resolution melting (HRM) re-analysis of a polyposis patients cohort reveals previously undetected heterozygous and mosaic APC gene mutations.
- Published in:
- Familial Cancer, 2015, v. 14, n. 2, p. 247, doi. 10.1007/s10689-015-9780-5
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- Publication type:
- Article
14
Germline RAD51B truncating mutation in a family with cutaneous melanoma.
- Published in:
- Familial Cancer, 2015, v. 14, n. 2, p. 337, doi. 10.1007/s10689-015-9781-4
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- Publication type:
- Article
15
Defective DNA mismatch repair activity is common in sebaceous neoplasms, and may be an ineffective approach to screen for Lynch syndrome.
- Published in:
- Familial Cancer, 2015, v. 14, n. 2, p. 259, doi. 10.1007/s10689-015-9782-3
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- Publication type:
- Article
16
Erratum to: Mutations of HNRNPA0 and WIF1 predispose members of a large family to multiple cancers.
- Published in:
- 2015
- By:
- Publication type:
- Erratum
17
Mutations of HNRNPA0 and WIF1 predispose members of a large family to multiple cancers.
- Published in:
- Familial Cancer, 2015, v. 14, n. 2, p. 297, doi. 10.1007/s10689-014-9758-8
- By:
- Publication type:
- Article