| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
A comparison of cosegregation analysis methods for the clinical setting
|
Rañola, John Michael O.
|
|
2017
|
17 |
2 |
p. 295-302
|
article
|
| 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
|
article
|
| 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
|
article
|
| 4 |
Cancer patients’ intentions towards receiving unsolicited genetic information obtained using next-generation sequencing
|
Bijlsma, Rhodé M.
|
|
2017
|
17 |
2 |
p. 309-316
|
article
|
| 5 |
Dental anomalies in pediatric patients with familial adenomatous polyposis
|
Septer, Seth
|
|
2017
|
17 |
2 |
p. 229-234
|
article
|
| 6 |
Discovery of mutations in homologous recombination genes in African-American women with breast cancer
|
Ding, Yuan Chun
|
|
2017
|
17 |
2 |
p. 187-195
|
article
|
| 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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 10 |
Mutational analysis of the RB1 gene and the inheritance patterns of retinoblastoma in Jordan
|
Yousef, Yacoub A.
|
|
2017
|
17 |
2 |
p. 261-268
|
article
|
| 11 |
Novel BRCA1 splice-site mutation in ovarian cancer patients of Slavic origin
|
Krivokuca, Ana
|
|
2017
|
17 |
2 |
p. 179-185
|
article
|
| 12 |
Pancreatic adenocarcinoma with a germline PTEN p.Arg234Gln mutation
|
Uemura, Sunao
|
|
2017
|
17 |
2 |
p. 255-259
|
article
|
| 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
|
article
|
| 14 |
p53 signaling pathway polymorphisms, cancer risk and tumor phenotype in TP53 R337H mutation carriers
|
Macedo, Gabriel S.
|
|
2017
|
17 |
2 |
p. 269-274
|
article
|
| 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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 18 |
Sporadic endometrial adenocarcinoma with MMR deficiency due to biallelic MSH2 somatic mutations
|
Buecher, Bruno
|
|
2017
|
17 |
2 |
p. 281-285
|
article
|
| 19 |
The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genes
|
Slavin, Thomas P.
|
|
2017
|
17 |
2 |
p. 235-245
|
article
|
| 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
|
article
|
Journal description