| 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
|
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