| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of Rothmund-Thomson syndrome originally thought to be a case of Bloom syndrome
|
Marmolejo Castañeda, David Humberto
|
|
|
22 |
1 |
p. 99-102
|
artikel
|
| 2 |
A large family with MSH3-related polyposis
|
Aelvoet, Arthur S.
|
|
|
22 |
1 |
p. 49-54
|
artikel
|
| 3 |
Endoscopic management of familial adenomatous polyposis targeting colorectal lesions greater than 5 mm in size: a single-center retrospective study
|
Murano, Tatsuro
|
|
|
22 |
1 |
p. 83-89
|
artikel
|
| 4 |
Founder vs. non-founder BRCA1/2 pathogenic alleles: the analysis of Belarusian breast and ovarian cancer patients and review of other studies on ethnically homogenous populations
|
Yanus, G. A.
|
|
|
22 |
1 |
p. 19-30
|
artikel
|
| 5 |
Healthcare professionals’ perspectives on implementation of universal tumor DNA testing in ovarian cancer patients: multidisciplinary focus groups
|
Witjes, Vera M.
|
|
|
22 |
1 |
p. 1-11
|
artikel
|
| 6 |
Hepatocellular carcinoma and solid pseudopapillary neoplasm of the pancreas complicating familial adenomatous polyposis: two cases and review of the literature
|
El Halabi, Jessica
|
|
|
22 |
1 |
p. 77-82
|
artikel
|
| 7 |
Mainstreaming germline genetic testing for patients with pancreatic cancer increases uptake
|
Ramsey, Mitchell L.
|
|
|
22 |
1 |
p. 91-97
|
artikel
|
| 8 |
Molecular characterization of an embryonal rhabdomyosarcoma occurring in a patient with Kabuki syndrome: report and literature review in the light of tumor predisposition syndromes
|
Aukema, Sietse M.
|
|
|
22 |
1 |
p. 103-118
|
artikel
|
| 9 |
Potential risks associated with the use of ionizing radiation for imaging and treatment of colorectal cancer in Lynch syndrome patients
|
Sun, Mingzhu
|
|
|
22 |
1 |
p. 61-70
|
artikel
|
| 10 |
Preimplantation genetic testing in patients with genetic susceptibility to cancer
|
Villy, Marie-Charlotte
|
|
|
22 |
1 |
p. 119-125
|
artikel
|
| 11 |
Prevalence and risk factors of barrett’s esophagus in lynch syndrome
|
Farha, Natalie
|
|
|
22 |
1 |
p. 55-60
|
artikel
|
| 12 |
Prevalence of FANCM germline variants in BRCA1/2 negative breast and/or ovarian cancer patients from Pakistan
|
Rashid, Muhammad Usman
|
|
|
22 |
1 |
p. 31-41
|
artikel
|
| 13 |
Remote vs in-person BRCA1/2 non-carriers test disclosure: patients’ choice during Covid-19 pandemic restriction
|
Costanzo, Silvia
|
|
|
22 |
1 |
p. 43-48
|
artikel
|
| 14 |
Truncating TINF2 p.Tyr312Ter variant and inherited breast cancer susceptibility
|
Koivuluoma, Susanna
|
|
|
22 |
1 |
p. 13-17
|
artikel
|
| 15 |
Universal tumor screening for lynch syndrome on colorectal cancer biopsies impacts surgical treatment decisions
|
Vazzano, Jennifer
|
|
|
22 |
1 |
p. 71-76
|
artikel
|
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