Found: 18
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Prospective enteroscopic evaluation of jejunal polyposis in patients with familial adenomatous polyposis and advanced duodenal polyposis.
- Published in:
- Familial Cancer, 2013, v. 12, n. 1, p. 51, doi. 10.1007/s10689-012-9571-1
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- Publication type:
- Article
The prevalence of BRCA mutations among familial breast cancer patients in Korea: results of the Korean Hereditary Breast Cancer study.
- Published in:
- Familial Cancer, 2013, v. 12, n. 1, p. 75, doi. 10.1007/s10689-012-9578-7
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- Publication type:
- Article
Birt-Hogg-Dubé: beyond the clinical manifestations.
- Published in:
- Familial Cancer, 2013, v. 12, n. 1, p. 97, doi. 10.1007/s10689-012-9583-x
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- Publication type:
- Article
Somatic mosaicism and double somatic hits can lead to MSI colorectal tumors.
- Published in:
- Familial Cancer, 2013, v. 12, n. 1, p. 27, doi. 10.1007/s10689-012-9568-9
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- Publication type:
- Article
Catalysts to withdrawal from familial ovarian cancer screening for surgery and reactions to discontinued screening: a qualitative study.
- Published in:
- Familial Cancer, 2013, v. 12, n. 1, p. 19, doi. 10.1007/s10689-012-9567-x
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- Publication type:
- Article
The spectrum of urological malignancy in Lynch syndrome.
- Published in:
- Familial Cancer, 2013, v. 12, n. 1, p. 57, doi. 10.1007/s10689-012-9573-z
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- Publication type:
- Article
An unusual BRCA mutation distribution in a high risk cancer genetics clinic.
- Published in:
- Familial Cancer, 2013, v. 12, n. 1, p. 83, doi. 10.1007/s10689-012-9581-z
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- Publication type:
- Article
Psychosocial factors and uptake of risk-reducing salpingo-oophorectomy in women at high risk for ovarian cancer.
- Published in:
- Familial Cancer, 2013, v. 12, n. 1, p. 101, doi. 10.1007/s10689-012-9585-8
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- Publication type:
- Article
Absence of loss of heterozygosity of BRCA1 in a renal tumor from a BRCA1 germline mutation carrier.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Feasibility evaluation of an online tool to guide decisions for BRCA1/2 mutation carriers.
- Published in:
- Familial Cancer, 2013, v. 12, n. 1, p. 65, doi. 10.1007/s10689-012-9577-8
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- Publication type:
- Article
Multiple small 'imaging' branch-duct type intraductal papillary mucinous neoplasms (IPMNs) in familial pancreatic cancer: indicator for concomitant high grade pancreatic intraepithelial neoplasia?
- Published in:
- Familial Cancer, 2013, v. 12, n. 1, p. 89, doi. 10.1007/s10689-012-9582-y
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- Publication type:
- Article
Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature review.
- Published in:
- Familial Cancer, 2013, v. 12, n. 1, p. 43, doi. 10.1007/s10689-012-9570-2
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- Publication type:
- Article
10 rare tumors that warrant a genetics referral.
- Published in:
- Familial Cancer, 2013, v. 12, n. 1, p. 1, doi. 10.1007/s10689-012-9584-9
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- Publication type:
- Article
The deletion of exons 3-5 of BRCA1 is the first founder rearrangement identified in breast and/or ovarian cancer Spanish families.
- Published in:
- Familial Cancer, 2013, v. 12, n. 1, p. 119, doi. 10.1007/s10689-012-9579-6
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- Publication type:
- Article
Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families.
- Published in:
- Familial Cancer, 2013, v. 12, n. 1, p. 35, doi. 10.1007/s10689-012-9569-8
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- Publication type:
- Article
A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts.
- Published in:
- Familial Cancer, 2013, v. 12, n. 1, p. 111, doi. 10.1007/s10689-012-9586-7
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- Publication type:
- Article
The Fourth Birt-Hogg-Dubé Symposium, Cincinnati, USA, 28-30 March, 2012.
- Published in:
- Familial Cancer, 2013, v. 12, n. 1, p. 133, doi. 10.1007/s10689-012-9528-4
- Publication type:
- Article
Value of bilateral breast cancer for identification of rare recessive at-risk alleles: evidence for the role of homozygous GEN1 c.2515_2519delAAGTT mutation.
- Published in:
- 2013
- By:
- Publication type:
- Letter