| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A mosaic pathogenic variant in MSH6 causes MSH6-deficient colorectal and endometrial cancer in a patient classified as suspected Lynch syndrome: a case report
|
Walker, Romy
|
|
|
22 |
4 |
p. 423-428
|
artikel
|
| 2 |
Balancing the burden and benefits of colonoscopy in Lynch Syndrome
|
Macrae, Finlay
|
|
|
22 |
4 |
p. 399-401
|
artikel
|
| 3 |
Cancer surveillance for transgender and gender diverse patients with Lynch syndrome: a practice resource of the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer
|
Hodan, Rachel
|
|
|
22 |
4 |
p. 437-448
|
artikel
|
| 4 |
Clinical and imaging modality factors impacting radiological interpretation of breast screening in young women with neurofibromatosis type 1
|
Wilding, Mathilda
|
|
|
22 |
4 |
p. 499-511
|
artikel
|
| 5 |
Colonoscopy surveillance in Lynch syndrome is burdensome and frequently delayed
|
van Liere, Elsa L. S. A.
|
|
|
22 |
4 |
p. 403-411
|
artikel
|
| 6 |
Combining clinical and molecular characterization of CDH1: a multidisciplinary approach to reclassification of a splicing variant
|
Fillman, Corrine
|
|
|
22 |
4 |
p. 521-526
|
artikel
|
| 7 |
Endoscopic and chemopreventive management of familial adenomatous polyposis syndrome
|
Stone, J. K.
|
|
|
22 |
4 |
p. 413-422
|
artikel
|
| 8 |
Germline whole genome sequencing in adults with multiple primary tumors
|
Wang, Yiming
|
|
|
22 |
4 |
p. 513-520
|
artikel
|
| 9 |
In deep bioinformatic characterization of a novel fumarate hydratase variant FH c.199T > G; (p.Tyr67Asp) in hereditary leiomyomatosis and renal cell carcinoma
|
Chami, Anisse
|
|
|
22 |
4 |
p. 481-486
|
artikel
|
| 10 |
Mainstreamed genetic testing of breast cancer patients: experience from a single surgeon’s practice in a large US Academic Center
|
Chai, Teresa S.
|
|
|
22 |
4 |
p. 467-474
|
artikel
|
| 11 |
PREMM5 distinguishes sporadic from Lynch syndrome-associated MMR-deficient/MSI-high colorectal cancer
|
Sandoval, Renata L.
|
|
|
22 |
4 |
p. 459-465
|
artikel
|
| 12 |
Prevalence and genetic spectrum associated with hereditary colorectal cancer syndromes, the need to improve cancer risk awareness, and family cascade testing in Vietnam
|
Nguyen, Huu-Thinh
|
|
|
22 |
4 |
p. 449-458
|
artikel
|
| 13 |
Reclassification of two germline DICER1 splicing variants leads to DICER1 syndrome diagnosis
|
Apellaniz-Ruiz, Maria
|
|
|
22 |
4 |
p. 487-493
|
artikel
|
| 14 |
Unusual phenotypes in patients with a pathogenic germline variant in DICER1
|
Venger, Kateryna
|
|
|
22 |
4 |
p. 475-480
|
artikel
|
| 15 |
Whole genome sequencing and disease pattern in patients with juvenile polyposis syndrome: a nationwide study
|
Jelsig, Anne Marie
|
|
|
22 |
4 |
p. 429-436
|
artikel
|
| 16 |
Willingness of individuals with Li-Fraumeni syndrome to participate in a cancer prevention trial: a survey study
|
Struewe, Farina J.
|
|
|
22 |
4 |
p. 495-497
|
artikel
|
Tijdschrift beschrijving