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
- By:
- Publication type:
- Article
Works matching IS 13899600 AND DT 2017 AND VI 16 AND IP 2
Results: 20
1
2
Cystic parathyroid glands in MEN1: A rare entity?
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 249, doi. 10.1007/s10689-016-9936-y
- By:
- Publication type:
- Article
3
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
- By:
- Publication type:
- Article
4
Attenuated polyposis of the large bowel: a morphologic and molecular approach.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 211, doi. 10.1007/s10689-016-9938-9
- By:
- Publication type:
- Article
5
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
- By:
- Publication type:
- Article
6
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
- By:
- Publication type:
- Article
7
A case of multiple gastrointestinal stromal tumors caused by a germline KIT gene mutation (p.Leu576Pro).
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 267, doi. 10.1007/s10689-016-9941-1
- By:
- Publication type:
- Article
8
Risk algorithms that include pathology adjustment for HER2 amplification need to make further downward adjustments in likelihood scores.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 173, doi. 10.1007/s10689-016-9942-0
- By:
- Publication type:
- Article
9
Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 271, doi. 10.1007/s10689-016-9943-z
- By:
- Publication type:
- Article
10
Analysis of a RECQL splicing mutation, c.1667_1667+3delAGTA, in breast cancer patients and controls from Central Europe.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 181, doi. 10.1007/s10689-016-9944-y
- By:
- Publication type:
- Article
11
Truncation of the MSH2 C-terminal 60 amino acids disrupts effective DNA mismatch repair and is causative for Lynch syndrome.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 221, doi. 10.1007/s10689-016-9945-x
- By:
- Publication type:
- Article
12
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
- By:
- Publication type:
- Article
13
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
- By:
- Publication type:
- Article
14
All in the family? Analyzing the impact of family history in addition to genotype on medullary thyroid carcinoma aggressiveness in MEN2A patients.
- Published in:
- Familial Cancer, 2017, v. 16, n. 2, p. 283, doi. 10.1007/s10689-016-9948-7
- By:
- Publication type:
- Article
15
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
- By:
- Publication type:
- Article
16
Colonoscopy in Lynch syndrome: the need for a new quality score.
- Published in:
- 2017
- By:
- Publication type:
- Letter
17
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
- By:
- Publication type:
- Article
18
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
- By:
- Publication type:
- Article
19
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
- By:
- Publication type:
- Article
20
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
- By:
- Publication type:
- Article