Works matching IS 13899600 AND DT 2014 AND VI 13 AND IP 1
Results: 16
Genetic variation at 8q24, family history of cancer, and upper gastrointestinal cancers in a Chinese population.
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- Familial Cancer, 2014, v. 13, n. 1, p. 45, doi. 10.1007/s10689-013-9673-4
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- Article
Lack of association between let-7 binding site polymorphism rs712 and risk of nasopharyngeal carcinoma.
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- Familial Cancer, 2014, v. 13, n. 1, p. 93, doi. 10.1007/s10689-013-9681-4
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- Article
Mammographic surveillance in women aged 35-39 at enhanced familial risk of breast cancer (FH02).
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- Familial Cancer, 2014, v. 13, n. 1, p. 13, doi. 10.1007/s10689-013-9661-8
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- Article
No evidence of genetic anticipation in a large family with Lynch syndrome.
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- Familial Cancer, 2014, v. 13, n. 1, p. 29, doi. 10.1007/s10689-013-9669-0
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- Article
Diversity of the clinical presentation of the MMR gene biallelic mutations.
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- Familial Cancer, 2014, v. 13, n. 1, p. 131, doi. 10.1007/s10689-013-9676-1
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Cancer risk and genotype-phenotype correlations in PTEN hamartoma tumor syndrome.
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- Familial Cancer, 2014, v. 13, n. 1, p. 57, doi. 10.1007/s10689-013-9674-3
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- Article
Does and should breast cancer genetic counselling include lifestyle advice?
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- Familial Cancer, 2014, v. 13, n. 1, p. 35, doi. 10.1007/s10689-013-9672-5
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- Article
Reflex testing for Lynch syndrome: If we build it, will they come? Lessons learned from the uptake of clinical genetics services by individuals with newly diagnosed colorectal cancer (CRC).
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- Familial Cancer, 2014, v. 13, n. 1, p. 75, doi. 10.1007/s10689-013-9677-0
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- Article
The MDM2 285G-309G haplotype is associated with an earlier age of tumour onset in patients with Li-Fraumeni syndrome.
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- Familial Cancer, 2014, v. 13, n. 1, p. 127, doi. 10.1007/s10689-013-9667-2
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- Article
MAX mutations status in Swedish patients with pheochromocytoma and paraganglioma tumours.
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- Familial Cancer, 2014, v. 13, n. 1, p. 121, doi. 10.1007/s10689-013-9666-3
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Cancer risk and overall survival in mismatch repair proficient hereditary non-polyposis colorectal cancer, Lynch syndrome and sporadic colorectal cancer.
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- Familial Cancer, 2014, v. 13, n. 1, p. 109, doi. 10.1007/s10689-013-9683-2
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- Article
The prevalence of small intestinal polyps in patients with familial adenomatous polyposis: a prospective capsule endoscopy study.
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- Familial Cancer, 2014, v. 13, n. 1, p. 23, doi. 10.1007/s10689-013-9668-1
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- Article
Illness perceptions, risk perception and worry in SDH mutation carriers.
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- Familial Cancer, 2014, v. 13, n. 1, p. 83, doi. 10.1007/s10689-013-9680-5
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- Article
Lynch Syndrome in high risk Ashkenazi Jews in Israel.
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- Familial Cancer, 2014, v. 13, n. 1, p. 65, doi. 10.1007/s10689-013-9675-2
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- Article
Endometrial tumour BRAF mutations and MLH1 promoter methylation as predictors of germline mismatch repair gene mutation status: a literature review.
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- Familial Cancer, 2014, v. 13, n. 1, p. 1, doi. 10.1007/s10689-013-9671-6
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- Article
Impact of breast cancer family history on tumor detection and tumor size in women newly-diagnosed with invasive breast cancer.
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- Familial Cancer, 2014, v. 13, n. 1, p. 99, doi. 10.1007/s10689-013-9682-3
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- Article