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                             16 gevonden resultaten
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
                             16 gevonden resultaten
 
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