The prevalence of germ-line TP53 mutations in women diagnosed with breast cancer before age 30.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 563, doi. 10.1007/s10689-009-9287-z
- By:
- Publication type:
- Article
Works matching IS 13899600 AND DT 2009 AND VI 8 AND IP 4
Results: 41
1
2
Functional characterization of rare missense mutations in MLH1 and MSH2 identified in Danish colorectal cancer patients.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 489, doi. 10.1007/s10689-009-9274-4
- By:
- Publication type:
- Article
3
The correlation between a family history of colorectal cancer and survival of patients with colorectal cancer.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 555, doi. 10.1007/s10689-009-9286-0
- By:
- Publication type:
- Article
4
p53 tetramerization domain mutations: germline R342X and R342P, and somatic R337G identified in pediatric patients with Li–Fraumeni syndrome and a child with adrenocortical carcinoma.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 541, doi. 10.1007/s10689-009-9284-2
- By:
- Publication type:
- Article
5
FAP-associated desmoid invasiveness correlates with in vitro resistance to doxorubicin.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 569, doi. 10.1007/s10689-009-9288-y
- By:
- Publication type:
- Article
6
Patient preferences and National Health Service costs: a cost-consequences analysis of cancer genetic services.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 265, doi. 10.1007/s10689-008-9217-5
- By:
- Publication type:
- Article
7
Mutation screening of VHL gene in a family with malignant bilateral pheochromocytoma: from isolated familial pheochromocytoma to von Hippel-Lindau disease.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 465, doi. 10.1007/s10689-009-9266-4
- By:
- Publication type:
- Article
8
Are prediction models for Lynch syndrome valid for probands with endometrial cancer?
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 483, doi. 10.1007/s10689-009-9273-5
- By:
- Publication type:
- Article
9
Identification of a de novo BRCA1 mutation in a woman with early onset bilateral breast cancer.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 479, doi. 10.1007/s10689-009-9270-8
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- Publication type:
- Article
10
Haplotypes of the I157T CHEK2 germline mutation in ethnically diverse populations.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 473, doi. 10.1007/s10689-009-9269-1
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- Publication type:
- Article
11
Screening for germline mutations of MLH1, MSH2, MSH6 and PMS2 genes in Slovenian colorectal cancer patients: implications for a population specific detection strategy of Lynch syndrome.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 421, doi. 10.1007/s10689-009-9258-4
- By:
- Publication type:
- Article
12
CHEK2*1100delC does not contribute to risk to breast cancer among Malay, Chinese and Indians in Malaysia.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 355, doi. 10.1007/s10689-009-9244-x
- By:
- Publication type:
- Article
13
Genetic testing for Lynch syndrome in the first year of colorectal cancer: a review of the psychological impact.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 325, doi. 10.1007/s10689-009-9239-7
- By:
- Publication type:
- Article
14
PALB2 sequence variants in young South African breast cancer patients.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 347, doi. 10.1007/s10689-009-9241-0
- By:
- Publication type:
- Article
15
Germline MLH1 and MSH2 mutations in Italian pancreatic cancer patients with suspected Lynch syndrome.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 547, doi. 10.1007/s10689-009-9285-1
- By:
- Publication type:
- Article
16
Molecular study of CEPBA in familial hematological malignancies.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 581, doi. 10.1007/s10689-009-9289-x
- By:
- Publication type:
- Article
17
A study on MSH2 and MLH1 mutations in hereditary nonpolyposis colorectal cancer families from the Basque Country, describing four new germline mutations.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 533, doi. 10.1007/s10689-009-9283-3
- By:
- Publication type:
- Article
18
TP53 germline mutations in Portugal and genetic modifiers of age at cancer onset.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 383, doi. 10.1007/s10689-009-9251-y
- By:
- Publication type:
- Article
19
Survey of unaffected BRCA and mismatch repair (MMR) mutation positive individuals.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 363, doi. 10.1007/s10689-009-9248-6
- By:
- Publication type:
- Article
20
Methylation not a frequent “second hit” in tumors with germline BRCA mutations.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 339, doi. 10.1007/s10689-009-9240-1
- By:
- Publication type:
- Article
21
Cancer prevention and screening practices among women at risk for hereditary breast and ovarian cancer after genetic counseling in the community setting.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 277, doi. 10.1007/s10689-009-9242-z
- By:
- Publication type:
- Article
22
Characterization of the largest kindred with MEN2A due to a Cys609Ser RET mutation.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 379, doi. 10.1007/s10689-009-9250-z
- By:
- Publication type:
- Article
23
Protective effect of copy number polymorphism of glutathione S-transferase T1 gene on melanoma risk in presence of CDKN2A mutations, MC1R variants and host-related phenotypes.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 371, doi. 10.1007/s10689-009-9249-5
- By:
- Publication type:
- Article
24
Improvement of endometrial biopsy over transvaginal ultrasound alone for endometrial surveillance in women with Lynch syndrome.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 391, doi. 10.1007/s10689-009-9252-x
- By:
- Publication type:
- Article
25
A high frequent BRCA1 founder mutation identified in the Greenlandic population.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 413, doi. 10.1007/s10689-009-9257-5
- By:
- Publication type:
- Article
26
Strategies for endometrial screening in the Lynch syndrome population: a patient acceptability study.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 431, doi. 10.1007/s10689-009-9259-3
- By:
- Publication type:
- Article
27
The RNF146 and ECHDC1 genes as candidates for inherited breast and ovarian cancer in Jewish Ashkenazi women.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 399, doi. 10.1007/s10689-009-9255-7
- By:
- Publication type:
- Article
28
Cancer genetic predisposition: information needs of patients irrespective of risk level.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 403, doi. 10.1007/s10689-009-9256-6
- By:
- Publication type:
- Article
29
First case report of Muir–Torre syndrome associated with non-small cell lung cancer.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 359, doi. 10.1007/s10689-009-9247-7
- By:
- Publication type:
- Article
30
Conflict between values and technology: perceptions of preimplantation genetic diagnosis among women at increased risk for hereditary breast and ovarian cancer.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 441, doi. 10.1007/s10689-009-9263-7
- By:
- Publication type:
- Article
31
Younger age-at-diagnosis for familial malignant testicular germ cell tumor.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 451, doi. 10.1007/s10689-009-9264-6
- By:
- Publication type:
- Article
32
Genetic polymorphism in ornithine decarboxylase and risk of breast cancer.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 307, doi. 10.1007/s10689-009-9237-9
- By:
- Publication type:
- Article
33
The relationship between knowledge of family history and cancer characteristics at diagnosis in women newly-diagnosed with invasive breast cancer.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 299, doi. 10.1007/s10689-009-9236-x
- By:
- Publication type:
- Article
34
Low contribution of BRCA1/2 genomic rearrangement to high-risk breast cancer in the Korean population.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 505, doi. 10.1007/s10689-009-9279-z
- By:
- Publication type:
- Article
35
Impact of 226C>T MSH2 gene mutation on cancer phenotypes in two HNPCC-associated highly-consanguineous families from Kuwait: emphasis on premarital genetic testing.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 289, doi. 10.1007/s10689-009-9275-3
- By:
- Publication type:
- Article
36
Epitope-positive truncating MLH1 mutation and loss of PMS2: implications for IHC-directed genetic testing for lynch syndrome.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 501, doi. 10.1007/s10689-009-9276-2
- By:
- Publication type:
- Article
37
Association of MUTYH and MSH6 germline mutations in colorectal cancer patients.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 525, doi. 10.1007/s10689-009-9282-4
- By:
- Publication type:
- Article
38
Determination of splice-site mutations in Lynch syndrome (hereditary non-polyposis colorectal cancer) patients using functional splicing assay.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 509, doi. 10.1007/s10689-009-9280-6
- By:
- Publication type:
- Article
39
Cancer risk in a cohort of subjects carrying a single mismatch repair gene mutation.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 519, doi. 10.1007/s10689-009-9281-5
- By:
- Publication type:
- Article
40
Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 313, doi. 10.1007/s10689-009-9238-8
- By:
- Publication type:
- Article
41
Attitude towards pre-implantation genetic diagnosis for hereditary cancer.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 457, doi. 10.1007/s10689-009-9265-5
- By:
- Publication type:
- Article