nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A comparison of cosegregation analysis methods for the clinical setting
|
Rañola, John Michael O. |
|
2017 |
17 |
2 |
p. 295-302 |
artikel |
2 |
A germline missense mutation in exon 3 of the MSH2 gene in a Lynch syndrome family: correlation with phenotype and localization assay
|
Bianchi, Francesca |
|
2017 |
17 |
2 |
p. 215-224 |
artikel |
3 |
A new hereditary colorectal cancer network in the Middle East and eastern mediterranean countries to improve care for high-risk families
|
Ghorbanoghli, Zeinab |
|
2017 |
17 |
2 |
p. 209-212 |
artikel |
4 |
Cancer patients’ intentions towards receiving unsolicited genetic information obtained using next-generation sequencing
|
Bijlsma, Rhodé M. |
|
2017 |
17 |
2 |
p. 309-316 |
artikel |
5 |
Dental anomalies in pediatric patients with familial adenomatous polyposis
|
Septer, Seth |
|
2017 |
17 |
2 |
p. 229-234 |
artikel |
6 |
Discovery of mutations in homologous recombination genes in African-American women with breast cancer
|
Ding, Yuan Chun |
|
2017 |
17 |
2 |
p. 187-195 |
artikel |
7 |
Erratum to: A new hereditary colorectal cancer network in the Middle East and eastern Mediterranean countries to improve care for high-risk families
|
Ghorbanoghli, Zeinab |
|
2017 |
17 |
2 |
p. 213 |
artikel |
8 |
Immunohistochemical null-phenotype for mismatch repair proteins in colonic carcinoma associated with concurrent MLH1 hypermethylation and MSH2 somatic mutations
|
Wang, Tao |
|
2017 |
17 |
2 |
p. 225-228 |
artikel |
9 |
Issues related to family history of cancer at the end of life: a palliative care providers’ survey
|
Gonthier, Catherine |
|
2017 |
17 |
2 |
p. 303-307 |
artikel |
10 |
Mutational analysis of the RB1 gene and the inheritance patterns of retinoblastoma in Jordan
|
Yousef, Yacoub A. |
|
2017 |
17 |
2 |
p. 261-268 |
artikel |
11 |
Novel BRCA1 splice-site mutation in ovarian cancer patients of Slavic origin
|
Krivokuca, Ana |
|
2017 |
17 |
2 |
p. 179-185 |
artikel |
12 |
Pancreatic adenocarcinoma with a germline PTEN p.Arg234Gln mutation
|
Uemura, Sunao |
|
2017 |
17 |
2 |
p. 255-259 |
artikel |
13 |
Pancreatic neuroendocrine tumor in a patient with a TSC1 variant: case report and review of the literature
|
Mortaji, Parisa |
|
2017 |
17 |
2 |
p. 275-280 |
artikel |
14 |
p53 signaling pathway polymorphisms, cancer risk and tumor phenotype in TP53 R337H mutation carriers
|
Macedo, Gabriel S. |
|
2017 |
17 |
2 |
p. 269-274 |
artikel |
15 |
Remarkable effects of imatinib in a family with young onset gastrointestinal stromal tumors and cutaneous hyperpigmentation associated with a germline KIT-Trp557Arg mutation: case report and literature overview
|
Farag, S. |
|
2017 |
17 |
2 |
p. 247-253 |
artikel |
16 |
Screening for Lynch syndrome in young Saudi colorectal cancer patients using microsatellite instability testing and next generation sequencing
|
Alqahtani, Masood |
|
2017 |
17 |
2 |
p. 197-203 |
artikel |
17 |
Screening of BMPR1a for pathogenic mutations in familial colorectal cancer type X families from Newfoundland
|
Evans, Daniel R. |
|
2017 |
17 |
2 |
p. 205-208 |
artikel |
18 |
Sporadic endometrial adenocarcinoma with MMR deficiency due to biallelic MSH2 somatic mutations
|
Buecher, Bruno |
|
2017 |
17 |
2 |
p. 281-285 |
artikel |
19 |
The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genes
|
Slavin, Thomas P. |
|
2017 |
17 |
2 |
p. 235-245 |
artikel |
20 |
Whole body magnetic resonance imaging (WB-MRI) and brain MRI baseline surveillance in TP53 germline mutation carriers: experience from the Li-Fraumeni Syndrome Education and Early Detection (LEAD) clinic
|
Bojadzieva, Jasmina |
|
2017 |
17 |
2 |
p. 287-294 |
artikel |