Found: 18
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Preimplantation genetic diagnosis for inherited breast cancer: first clinical application and live birth in Spain.
- Published in:
- Familial Cancer, 2012, v. 11, n. 2, p. 175, doi. 10.1007/s10689-011-9497-z
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- Article
Validation of three BRCA1/ 2 mutation-carrier probability models Myriad, BRCAPRO and BOADICEA in a population-based series of 183 German families.
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- Familial Cancer, 2012, v. 11, n. 2, p. 181, doi. 10.1007/s10689-011-9498-y
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- Article
Looking different, feeling different: women's reactions to risk-reducing breast and ovarian surgery.
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- Familial Cancer, 2012, v. 11, n. 2, p. 215, doi. 10.1007/s10689-011-9504-4
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- Article
Management of duodenal adenomatosis in FAP: single centre experience.
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- Familial Cancer, 2012, v. 11, n. 2, p. 167, doi. 10.1007/s10689-011-9496-0
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- Article
A novel germline SDHB mutation in a gastrointestinal stromal tumor patient without bona fide features of the Carney-Stratakis dyad.
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- Familial Cancer, 2012, v. 11, n. 2, p. 189, doi. 10.1007/s10689-011-9499-x
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- Article
Urologists' and GPs' knowledge of hereditary prostate cancer is suboptimal for prostate cancer counseling: a nation-wide survey in The Netherlands.
- Published in:
- Familial Cancer, 2012, v. 11, n. 2, p. 195, doi. 10.1007/s10689-011-9500-8
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- Article
Hereditary medullary thyroid carcinoma: the management dilemma.
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- Familial Cancer, 2012, v. 11, n. 2, p. 157, doi. 10.1007/s10689-011-9501-7
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- Article
Analysis of the miR- 34a locus in 62 patients with familial cutaneous melanoma negative for CDKN2A/CDK4 screening.
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- Familial Cancer, 2012, v. 11, n. 2, p. 201, doi. 10.1007/s10689-011-9502-6
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- Article
Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutations.
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- Familial Cancer, 2012, v. 11, n. 2, p. 235, doi. 10.1007/s10689-011-9506-2
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- Article
The founder Ashkenazi Jewish mutations in the MSH2 and MSH6 genes in Israeli patients with gastric and pancreatic cancer.
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- Familial Cancer, 2012, v. 11, n. 2, p. 243, doi. 10.1007/s10689-011-9507-1
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- Article
Active surveillance of renal masses in von Hippel-Lindau disease: growth rates and clinical outcome over a median follow-up period of 56 months.
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- Familial Cancer, 2012, v. 11, n. 2, p. 209, doi. 10.1007/s10689-011-9503-5
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- Article
RB1 mutations and second primary malignancies after hereditary retinoblastoma.
- Published in:
- Familial Cancer, 2012, v. 11, n. 2, p. 225, doi. 10.1007/s10689-011-9505-3
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- Article
Psychological distress in newly diagnosed colorectal cancer patients following microsatellite instability testing for Lynch syndrome on the pathologist's initiative.
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- Familial Cancer, 2012, v. 11, n. 2, p. 259, doi. 10.1007/s10689-012-9510-1
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- Article
Can a gastrointestinal pathologist identify microsatellite instability in colorectal cancer with reproducibility and a high degree of specificity?
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- Familial Cancer, 2012, v. 11, n. 2, p. 249, doi. 10.1007/s10689-012-9508-8
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- Article
Prevalence of TP53 germ line mutations in young Pakistani breast cancer patients.
- Published in:
- Familial Cancer, 2012, v. 11, n. 2, p. 307, doi. 10.1007/s10689-012-9509-7
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- Article
Predictive genetic testing of first degree relatives of mutation carriers is a cost-effective strategy in preventing hereditary non-polyposis colorectal cancer in Singapore.
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- Familial Cancer, 2012, v. 11, n. 2, p. 279, doi. 10.1007/s10689-012-9513-y
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- Article
French women's breast self-examination practices with time after undergoing BRCA1/2 genetic testing.
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- Familial Cancer, 2012, v. 11, n. 2, p. 269, doi. 10.1007/s10689-012-9512-z
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- Publication type:
- Article
Families' experience of oncogenetic counselling: accounts from a heterogeneous hereditary cancer risk population.
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- Familial Cancer, 2012, v. 11, n. 2, p. 291, doi. 10.1007/s10689-012-9514-x
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- Article