Works matching IS 13899600 AND DT 2017 AND VI 16 AND IP 2
Results: 20
TP53 and CDKN1A mutation analysis in families with Li-Fraumeni and Li-Fraumeni like syndromes.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 243, doi. 10.1007/s10689-016-9935-z
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- Publication type:
- Article
Cystic parathyroid glands in MEN1: A rare entity?
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- Familial Cancer, 2017, v. 16, n. 2, p. 249, doi. 10.1007/s10689-016-9936-y
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- Publication type:
- Article
Pain evaluation during gynaecological surveillance in women with Lynch syndrome.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 205, doi. 10.1007/s10689-016-9937-x
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- Article
Attenuated polyposis of the large bowel: a morphologic and molecular approach.
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- Familial Cancer, 2017, v. 16, n. 2, p. 211, doi. 10.1007/s10689-016-9938-9
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- Publication type:
- Article
Truncation of the MSH2 C-terminal 60 amino acids disrupts effective DNA mismatch repair and is causative for Lynch syndrome.
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- Familial Cancer, 2017, v. 16, n. 2, p. 221, doi. 10.1007/s10689-016-9945-x
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- Publication type:
- Article
Uptake of genetic counseling, genetic testing and surveillance in hereditary malignant melanoma ( CDKN2A) in Norway.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 257, doi. 10.1007/s10689-016-9939-8
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- Publication type:
- Article
A case of multiple gastrointestinal stromal tumors caused by a germline KIT gene mutation (p.Leu576Pro).
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- Familial Cancer, 2017, v. 16, n. 2, p. 267, doi. 10.1007/s10689-016-9941-1
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- Publication type:
- Article
Risk algorithms that include pathology adjustment for HER2 amplification need to make further downward adjustments in likelihood scores.
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- Familial Cancer, 2017, v. 16, n. 2, p. 173, doi. 10.1007/s10689-016-9942-0
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- Publication type:
- Article
Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands.
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- Familial Cancer, 2017, v. 16, n. 2, p. 271, doi. 10.1007/s10689-016-9943-z
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- Publication type:
- Article
Analysis of a RECQL splicing mutation, c.1667_1667+3delAGTA, in breast cancer patients and controls from Central Europe.
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- Familial Cancer, 2017, v. 16, n. 2, p. 181, doi. 10.1007/s10689-016-9944-y
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- Publication type:
- Article
BRCA1 allele-specific expression in genetic predisposed breast/ovarian cancer.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 167, doi. 10.1007/s10689-016-9940-2
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- Article
Four generations of SDHB-related disease: complexities in management.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 279, doi. 10.1007/s10689-016-9946-9
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- Publication type:
- Article
Cancer screening behaviors and risk perceptions among family members of colorectal cancer patients with unexplained mismatch repair deficiency.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 231, doi. 10.1007/s10689-016-9947-8
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- Publication type:
- Article
All in the family? Analyzing the impact of family history in addition to genotype on medullary thyroid carcinoma aggressiveness in MEN2A patients.
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- Familial Cancer, 2017, v. 16, n. 2, p. 283, doi. 10.1007/s10689-016-9948-7
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- Publication type:
- Article
DICER1 mutation and tumors associated with a familial tumor predisposition syndrome: practical considerations.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 291, doi. 10.1007/s10689-016-9949-6
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- Publication type:
- Article
Colonoscopy in Lynch syndrome: the need for a new quality score.
- Published in:
- 2017
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- Publication type:
- Letter
Recurrent TP53 missense mutation in cancer patients of Arab descent.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 295, doi. 10.1007/s10689-016-9951-z
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- Publication type:
- Article
Double germline mutations in APC and BRCA2 in an individual with a pancreatic tumor.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 303, doi. 10.1007/s10689-016-9952-y
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- Publication type:
- Article
Efficacy versus effectiveness of clinical genetic testing criteria for BRCA1 and BRCA2 hereditary mutations in incident breast cancer.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 187, doi. 10.1007/s10689-016-9953-x
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- Publication type:
- Article
Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 195, doi. 10.1007/s10689-016-9934-0
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- Publication type:
- Article