nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
APC rearrangements in familial adenomatous polyposis: heterogeneity of deletion lengths and breakpoint sequences underlies similar phenotypes
|
Quadri, Marialuisa |
|
2014 |
14 |
1 |
p. 41-49 |
artikel |
2 |
Desmoid tumour in familial adenomatous polyposis patients: responses to treatments
|
Desurmont, Thibault |
|
2014 |
14 |
1 |
p. 31-39 |
artikel |
3 |
Detection of inherited mutations for hereditary cancer using target enrichment and next generation sequencing
|
Guan, Yanfang |
|
2014 |
14 |
1 |
p. 9-18 |
artikel |
4 |
Down-regulation of malignant potential by alpha linolenic acid in human and mouse colon cancer cells
|
Chamberland, John P. |
|
2014 |
14 |
1 |
p. 25-30 |
artikel |
5 |
Estimate of the penetrance of BRCA mutation and the COS software for the assessment of BRCA mutation probability
|
Berrino, Jacopo |
|
2014 |
14 |
1 |
p. 117-128 |
artikel |
6 |
Familial and sporadic pancreatic cancer share the same molecular pathogenesis
|
Norris, Alexis L. |
|
2014 |
14 |
1 |
p. 95-103 |
artikel |
7 |
Further evidence for pathogenicity of the TP53 tetramerization domain mutation p.Arg342Pro in Li–Fraumeni syndrome
|
Etzold, Anna |
|
2014 |
14 |
1 |
p. 161-165 |
artikel |
8 |
Gastric cancer in three relatives of a patient with a biallelic IL12RB1 mutation
|
Vogelaar, Ingrid P. |
|
2014 |
14 |
1 |
p. 89-94 |
artikel |
9 |
Gly322Asp and Asn127Ser single nucleotide polymorphisms (SNPs) of hMSH2 mismatch repair gene and the risk of triple-negative breast cancer in Polish women
|
Smolarz, Beata |
|
2014 |
14 |
1 |
p. 81-88 |
artikel |
10 |
Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutations
|
Ahlborn, Lise B. |
|
2014 |
14 |
1 |
p. 129-133 |
artikel |
11 |
Identification of a novel MSH6 germline variant in a family with multiple gastro-intestinal malignancies by next generation sequencing
|
Connor, Ashton A. |
|
2014 |
14 |
1 |
p. 69-75 |
artikel |
12 |
Long-term outcomes of risk-reducing surgery in unaffected women at increased familial risk of breast and/or ovarian cancer
|
Heiniger, Louise |
|
2014 |
14 |
1 |
p. 105-115 |
artikel |
13 |
Mismatch repair deficient-crypts in non-neoplastic colonic mucosa in Lynch syndrome: insights from an illustrative case
|
Shia, Jinru |
|
2014 |
14 |
1 |
p. 61-68 |
artikel |
14 |
Mitochondrial membrane potential and reactive oxygen species in cancer stem cells
|
Zhang, Bei-bei |
|
2014 |
14 |
1 |
p. 19-23 |
artikel |
15 |
MLH1 promotor hypermethylation does not rule out a diagnosis of Lynch syndrome: a case report
|
Raymond, Victoria M. |
|
2014 |
14 |
1 |
p. 77-80 |
artikel |
16 |
Multiple skin hamartomata: a possible novel clinical presentation of SUFU neoplasia syndrome
|
Mann, Kirsty |
|
2014 |
14 |
1 |
p. 151-155 |
artikel |
17 |
Outcomes of genetic evaluation for hereditary cancer syndromes in unaffected individuals
|
Gustafson, Shanna L. |
|
2014 |
14 |
1 |
p. 167-174 |
artikel |
18 |
Population-based genetic risk prediction and stratification for ovarian cancer: views from women at high risk
|
Rahman, Belinda |
|
2014 |
14 |
1 |
p. 135-144 |
artikel |
19 |
Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe
|
Bogdanova, Natalia |
|
2014 |
14 |
1 |
p. 145-149 |
artikel |
20 |
Single nucleotide polymorphisms in PDCD6 gene are associated with the development of cervical squamous cell carcinoma
|
Zhou, Bin |
|
2014 |
14 |
1 |
p. 1-8 |
artikel |
21 |
18th annual meeting: Collaborative Group of the Americas on Inherited Colorectal Cancer (CGA-ICC)
|
|
|
2014 |
14 |
1 |
p. 175-209 |
artikel |
22 |
The impact of risk-reducing gynaecological surgery in premenopausal women at high risk of endometrial and ovarian cancer due to Lynch syndrome
|
Moldovan, Ramona |
|
2014 |
14 |
1 |
p. 51-60 |
artikel |
23 |
Vestibular schwannoma in a patient with neurofibromatosis type 1: clinical report and literature review
|
Huq, Aamira |
|
2014 |
14 |
1 |
p. 157-160 |
artikel |