Works matching IS 13899600 AND DT 2010 AND VI 9
Results: 103
MYH biallelic mutation can inactivate the two genetic pathways of colorectal cancer by APC or MLH1 transversions.
- Published in:
- Familial Cancer, 2010, v. 9, n. 4, p. 589, doi. 10.1007/s10689-010-9367-0
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- Publication type:
- Article
Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations.
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- Familial Cancer, 2010, v. 9, n. 4, p. 625, doi. 10.1007/s10689-010-9356-3
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- Article
Complete BRCA mutation screening in breast and ovarian cancer predisposition families from a North-Eastern Romanian population.
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- Familial Cancer, 2010, v. 9, n. 4, p. 519, doi. 10.1007/s10689-010-9361-6
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- Article
Clinical and molecular characterization of Brazilian families with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation.
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- Familial Cancer, 2010, v. 9, n. 4, p. 635, doi. 10.1007/s10689-010-9357-2
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- Article
Magnetic resonance colonography for colorectal cancer screening in patients with Lynch syndrome gene mutation.
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- Familial Cancer, 2010, v. 9, n. 4, p. 555, doi. 10.1007/s10689-010-9350-9
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- Article
Breast cancer susceptibility variants alter risk in familial ovarian cancer.
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- Familial Cancer, 2010, v. 9, n. 4, p. 503, doi. 10.1007/s10689-010-9349-2
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- Article
Predicting BRCA1 and BRCA2 gene mutation carriers: comparison of PENN II model to previous study.
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- Familial Cancer, 2010, v. 9, n. 4, p. 495, doi. 10.1007/s10689-010-9348-3
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- Article
FAP, gastric cancer, and genetic counseling featuring children and young adults: a family study and review.
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- Familial Cancer, 2010, v. 9, n. 4, p. 581, doi. 10.1007/s10689-010-9352-7
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- Article
Report of the Combined Meeting of the International Society for Gastrointestinal Hereditary Tumours, the Human Variome Project and the National Cancer Institute Colon Cancer Family Registry, Duesseldorf, Germany, 24 June 2009.
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- 2010
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- Publication type:
- Report
Can a phenotype for recessive inheritance in breast cancer be defined?
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- Familial Cancer, 2010, v. 9, n. 4, p. 525, doi. 10.1007/s10689-010-9355-4
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- Article
Abstracts 3rd Biennial Meeting of InSiGHT (International Society for Gastrointestinal Hereditary Tumours).
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- Familial Cancer, 2010, v. 9, n. 4, p. 713, doi. 10.1007/s10689-010-9351-8
- Publication type:
- Article
A novel mutation of the Succinate Dehydrogenase B Gene in a Korean Family with Pheochromocytoma.
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- Familial Cancer, 2010, v. 9, n. 4, p. 643, doi. 10.1007/s10689-010-9359-0
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- Publication type:
- Article
Screening for large genomic rearrangements of the BRIP1 and CHK1 genes in Finnish breast cancer families.
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- Familial Cancer, 2010, v. 9, n. 4, p. 537, doi. 10.1007/s10689-010-9360-7
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- Publication type:
- Article
Peutz-Jeghers syndrome: a study of long-term surgical morbidity and causes of mortality.
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- Familial Cancer, 2010, v. 9, n. 4, p. 609, doi. 10.1007/s10689-010-9358-1
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- Publication type:
- Article
The contribution of breast cancer pathology to statistical models to predict mutation risk in BRCA carriers.
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- Familial Cancer, 2010, v. 9, n. 4, p. 545, doi. 10.1007/s10689-010-9362-5
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- Publication type:
- Article
Disclosing cancer genetic information within families: perspectives of counselees and their at-risk relatives.
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- Familial Cancer, 2010, v. 9, n. 4, p. 669, doi. 10.1007/s10689-010-9364-3
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- Publication type:
- Article
Selective COX-2 inhibition affects fatty acids, but not COX mRNA expression in patients with FAP.
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- Familial Cancer, 2010, v. 9, n. 4, p. 571, doi. 10.1007/s10689-010-9365-2
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- Article
Pancreatic cancer risk counselling and screening: impact on perceived risk and psychological functioning.
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- Familial Cancer, 2010, v. 9, n. 4, p. 617, doi. 10.1007/s10689-010-9354-5
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- Publication type:
- Article
Papillary thyroid cancer in a patient with MUTYH-associated polyposis (MAP).
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- Familial Cancer, 2010, v. 9, n. 4, p. 595, doi. 10.1007/s10689-010-9366-1
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- Publication type:
- Article
Regular surveillance for Li-fraumeni syndrome: advice, adherence and perceived benefits.
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- Familial Cancer, 2010, v. 9, n. 4, p. 647, doi. 10.1007/s10689-010-9368-z
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- Publication type:
- Article
A functional varient in microRNA-146a is associated with risk of esophageal squamous cell carcinoma in Chinese Han.
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- Familial Cancer, 2010, v. 9, n. 4, p. 599, doi. 10.1007/s10689-010-9370-5
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- Publication type:
- Article
Comprehensive BRCA1 and BRCA2 mutation analyses and review of French Canadian families with at least three cases of breast cancer.
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- Familial Cancer, 2010, v. 9, n. 4, p. 507, doi. 10.1007/s10689-010-9372-3
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- Publication type:
- Article
Frequency of extracolonic tumors in Brazilian families with Lynch syndrome: analysis of a hereditary colorectal cancer institutional registry.
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- Familial Cancer, 2010, v. 9, n. 4, p. 563, doi. 10.1007/s10689-010-9373-2
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- Publication type:
- Article
Similarities in solar ultraviolet irradiance and other environmental factors may explain much of the family link between uveal melanoma and other cancers.
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- 2010
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- Publication type:
- Letter
Thymoma associated with malignancies may herald a hereditary cancer syndrome.
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- 2010
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- Publication type:
- Letter
Hereditary predisposition rather than environmental factor are likely to explain the familial link between uveal melanoma and other cancers.
- Published in:
- 2010
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- Publication type:
- Letter
Real world experience with cancer genetic counseling via telephone.
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- Familial Cancer, 2010, v. 9, n. 4, p. 681, doi. 10.1007/s10689-010-9369-y
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- Publication type:
- Article
BRCA1 and BRCA2 families and the risk of skin cancer.
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- Familial Cancer, 2010, v. 9, n. 4, p. 489, doi. 10.1007/s10689-010-9377-y
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- Publication type:
- Article
CDH1 gene mutations do not contribute in hereditary diffuse gastric cancer in Poland.
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- Familial Cancer, 2010, v. 9, n. 4, p. 605, doi. 10.1007/s10689-010-9381-2
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- Publication type:
- Article
Contribution of CDKN2A/P16, P14, CDK4 and BRCA1/2 germline mutations in individuals with suspected genetic predisposition to uveal melanoma.
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- Familial Cancer, 2010, v. 9, n. 4, p. 663, doi. 10.1007/s10689-010-9379-9
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- Publication type:
- Article
PALB2: a novel inactivating mutation in a Italian breast cancer family.
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- Familial Cancer, 2010, v. 9, n. 4, p. 531, doi. 10.1007/s10689-010-9382-1
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- Publication type:
- Article
Communicating genetic risk information within families: a review.
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- Familial Cancer, 2010, v. 9, n. 4, p. 691, doi. 10.1007/s10689-010-9380-3
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- Publication type:
- Article
BRCA1 mutations and colorectal cancer in Poland.
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- Familial Cancer, 2010, v. 9, n. 4, p. 541, doi. 10.1007/s10689-010-9378-x
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- Publication type:
- Article
Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations.
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- Familial Cancer, 2010, v. 9, n. 3, p. 283, doi. 10.1007/s10689-010-9345-6
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- Publication type:
- Article
Detection of allelic imbalance in MLH1 expression by pyrosequencing serves as a tool for the identification of germline defects in Lynch syndrome.
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- Familial Cancer, 2010, v. 9, n. 3, p. 345, doi. 10.1007/s10689-009-9314-0
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- Publication type:
- Article
Pregnancy after prophylactic total gastrectomy.
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- Familial Cancer, 2010, v. 9, n. 3, p. 331, doi. 10.1007/s10689-009-9316-y
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- Publication type:
- Article
Update multiple endocrine neoplasia type 2.
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- Familial Cancer, 2010, v. 9, n. 3, p. 449, doi. 10.1007/s10689-010-9320-2
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- Article
High risk for neoplastic transformation of endometriosis in a carrier of lynch syndrome.
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- Familial Cancer, 2010, v. 9, n. 3, p. 383, doi. 10.1007/s10689-010-9321-1
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- Publication type:
- Article
“ I have always believed I was at high risk...” The role of expectation in emotional responses to the receipt of an average, moderate or high cancer genetic risk assessment result: a thematic analysis of free-text questionnaire comments.
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- Familial Cancer, 2010, v. 9, n. 3, p. 469, doi. 10.1007/s10689-010-9324-y
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- Publication type:
- Article
Carney triad versus Carney Stratakis syndrome: two cases which illustrate the difficulty in distinguishing between these conditions in individual patients.
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- Familial Cancer, 2010, v. 9, n. 3, p. 443, doi. 10.1007/s10689-010-9323-z
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- Publication type:
- Article
Can self-esteem, mastery and perceived stigma predict long-term adjustment in women carrying a BRCA1/2-mutation? Evidence from a multi-center study.
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- Familial Cancer, 2010, v. 9, n. 3, p. 305, doi. 10.1007/s10689-010-9325-x
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- Publication type:
- Article
Differences in clinical and pathological characteristics of colorectal cancer in Arab as compared to Jewish patients in Northern Israel.
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- Familial Cancer, 2010, v. 9, n. 3, p. 327, doi. 10.1007/s10689-010-9337-6
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- Publication type:
- Article
Assessment of clinical practices among cancer genetic counselors.
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- Familial Cancer, 2010, v. 9, n. 3, p. 459, doi. 10.1007/s10689-010-9326-9
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- Publication type:
- Article
RASSF1A polymorphism in familial breast cancer.
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- Familial Cancer, 2010, v. 9, n. 3, p. 263, doi. 10.1007/s10689-010-9335-8
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- Publication type:
- Article
Analysis of mismatch repair gene mutations in Turkish HNPCC patients.
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- Familial Cancer, 2010, v. 9, n. 3, p. 365, doi. 10.1007/s10689-010-9336-7
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- Publication type:
- Article
Atypical identification of Lynch syndrome by immunohistochemistry and microsatellite instability analysis on jejunal adenocarcinoma.
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- Familial Cancer, 2010, v. 9, n. 3, p. 377, doi. 10.1007/s10689-010-9339-4
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- Publication type:
- Article
Novel germline mutations in BRCA2 gene among breast and breast-ovarian cancer families from Poland.
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- Familial Cancer, 2010, v. 9, n. 3, p. 267, doi. 10.1007/s10689-010-9338-5
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- Publication type:
- Article
Relationship of BRCA1 and BRCA2 mutations with cancer burden in the family and tumor incidence.
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- Familial Cancer, 2010, v. 9, n. 3, p. 291, doi. 10.1007/s10689-010-9327-8
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- Publication type:
- Article
Uptake of predictive testing among relatives of BRCA1 and BRCA2 families: a multicenter study in northeastern Spain.
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- Familial Cancer, 2010, v. 9, n. 3, p. 297, doi. 10.1007/s10689-009-9313-1
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- Publication type:
- Article
A distinct mutation on the alternative splice site of APC exon 9 results in attenuated familial adenomatous polyposis phenotype.
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- Familial Cancer, 2010, v. 9, n. 3, p. 395, doi. 10.1007/s10689-009-9317-x
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- Publication type:
- Article