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                             20 results found
no title author magazine year volume issue page(s) type
1 Adaptation of couples living with a high risk of breast/ovarian cancer and the association with risk-reducing surgery Shapira, Rachel
2017
17 4 p. 485-493
article
2 APC mosaicism in a young woman with desmoid type fibromatosis and familial adenomatous polyposis Stormorken, Astrid Tenden
2018
17 4 p. 539-543
article
3 A retrospective review of 48 individuals, including 12 families, molecularly diagnosed with hereditary leiomyomatosis and renal cell cancer (HLRCC) Bhola, Priya T.
2018
17 4 p. 615-620
article
4 Clinical interpretation of pathogenic ATM and CHEK2 variants on multigene panel tests: navigating moderate risk West, Allison H.
2018
17 4 p. 495-505
article
5 Commentary: PREMM5 threshold of 2.5% is recommended to improve identification of PMS2 carriers Kastrinos, Fay
2018
17 4 p. 567
article
6 Correlation of IL-31 gene polymorphisms with susceptibility and clinical recurrence of bladder cancer Li, Qin
2017
17 4 p. 577-585
article
7 Discussions about predictive genetic testing for Lynch syndrome: the role of health professionals and families in decisions to decline Kanga-Parabia, Anaita
2018
17 4 p. 547-555
article
8 Feasibility of endoscopic resection using bipolar snare for nonampullary duodenal tumours in familial adenomatous polyposis patients Inoki, Kazuya
2017
17 4 p. 517-524
article
9 Gene expression analysis in peripheral blood cells of patients with hereditary leiomyomatosis and renal cell cancer syndrome (HLRCC): identification of NRF2 pathway activation Arenas Valencia, Carolina
2018
17 4 p. 587-599
article
10 Haplotype analysis suggest that the MLH1 c.2059C > T mutation is a Swedish founder mutation Salomé, Jenny von
2017
17 4 p. 531-537
article
11 Letter to the editor Anele, C. C.
2018
17 4 p. 565-566
article
12 Metachronous colorectal cancer following segmental or extended colectomy in Lynch syndrome: a systematic review and meta-analysis Malik, Salim S.
2017
17 4 p. 557-564
article
13 Molecular analysis of an asbestos-exposed Belgian family with a high prevalence of mesothelioma Hylebos, Marieke
2018
17 4 p. 569-576
article
14 Mutations in context: implications of BRCA testing in diverse populations Felix, Gabriela E. S.
2017
17 4 p. 471-483
article
15 Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same Huq, A. J.
2018
17 4 p. 601-606
article
16 Response to letter to editor regarding published article—metachronous colorectal cancer following segmental or extended colectomy in Lynch syndrome: a systematic review and meta-analysis Lythgoe, Mark P.
2018
17 4 p. 545-546
article
17 Risk management adherence following genetic testing for hereditary cancer syndromes: a Singaporean experience Courtney, Eliza
2018
17 4 p. 621-626
article
18 SNP association study in PMS2-associated Lynch syndrome Broeke, Sanne W. ten
2017
17 4 p. 507-515
article
19 The first two confirmed sub-Saharan African families with germline TP53 mutations causing Li-Fraumeni syndrome Macaulay, Shelley
2018
17 4 p. 607-613
article
20 Urological sequelae of desmoids associated with familial adenomatous polyposis Walton, S. J.
2018
17 4 p. 525-530
article
                             20 results found
 
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