| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A de novo pathogenic variant in the MSH6 gene in a 52 years-old woman
|
Pierre-Noël, Elise
|
|
|
21 |
3 |
p. 319-324
|
artikel
|
| 2 |
A patient with very early onset FH-deficient renal cell carcinoma diagnosed at age seven
|
Taniguchi, Rieko
|
|
|
21 |
3 |
p. 337-341
|
artikel
|
| 3 |
A recurrent pathogenic BRCA2 exon 5–11 duplication in the Christian Arab population in Israel
|
Reznick Levi, Gili
|
|
|
21 |
3 |
p. 289-294
|
artikel
|
| 4 |
Correction to: Outcomes of retesting in patients with previously uninformative cancer genetics evaluations
|
Dettwyler, Shenin A.
|
|
|
21 |
3 |
p. 387-388
|
artikel
|
| 5 |
Eighth International Symposium on hereditary breast and ovarian cancer
|
|
|
|
21 |
3 |
p. 255-288
|
artikel
|
| 6 |
Familial colorectal cancer and tooth agenesis caused by an AXIN2 variant: how do we detect families with rare cancer predisposition syndromes?
|
Jensen, Janni M.
|
|
|
21 |
3 |
p. 325-332
|
artikel
|
| 7 |
Fibroadenoma in vulval ectopic breast tissue in a patient with PTEN Hamartoma Tumour Syndrome
|
Dawson, Hannah
|
|
|
21 |
3 |
p. 363-368
|
artikel
|
| 8 |
Identification of women at risk of hereditary breast–ovarian cancer among participants in a population-based breast cancer screening
|
Bonelli, Luigina
|
|
|
21 |
3 |
p. 309-318
|
artikel
|
| 9 |
Novel MAPK/AKT-impairing germline NRAS variant identified in a melanoma-prone family
|
Brown, Kevin M.
|
|
|
21 |
3 |
p. 347-355
|
artikel
|
| 10 |
Outcomes of retesting in patients with previously uninformative cancer genetics evaluations
|
Dettwyler, Shenin A.
|
|
|
21 |
3 |
p. 375-385
|
artikel
|
| 11 |
Patient ethnicity and cascade genetic testing: a descriptive study of a publicly funded hereditary cancer program
|
Braley, Eryn F.
|
|
|
21 |
3 |
p. 369-374
|
artikel
|
| 12 |
Positive experiences of healthcare professionals with a mainstreaming approach of germline genetic testing for women with ovarian cancer
|
Bokkers, Kyra
|
|
|
21 |
3 |
p. 295-304
|
artikel
|
| 13 |
PTCH2 is not a strong candidate gene for gorlin syndrome predisposition
|
Smith, Miriam J.
|
|
|
21 |
3 |
p. 343-346
|
artikel
|
| 14 |
Re-evaluating cancer risks associated with the CHEK2 p.Ser428Phe Ashkenazi Jewish founder pathogenic variant
|
Laitman, Yael
|
|
|
21 |
3 |
p. 305-308
|
artikel
|
| 15 |
Uterine leiomyomatosis in adolescents and young adults (AYAs) may represent a narrow phenotypic variant of FH tumour predisposition syndrome
|
Foo, Tiffany
|
|
|
21 |
3 |
p. 357-362
|
artikel
|
| 16 |
Utility of interim blood tests for cancer screening in Li-Fraumeni syndrome
|
Oba, Leatrisse
|
|
|
21 |
3 |
p. 333-336
|
artikel
|
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