Works matching IS 13899600 AND DT 2018 AND VI 17 AND IP 4

Results: 20

Molecular analysis of an asbestos-exposed Belgian family with a high prevalence of mesothelioma.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 569, doi. 10.1007/s10689-018-0095-1
By:
- Hylebos, Marieke;
- Op de Beeck, Ken;
- van den Ende, Jenneke;
- Pauwels, Patrick;
- Lammens, Martin;
- van Meerbeeck, Jan P.;
- Van Camp, Guy
Publication type:
Article
Discussions about predictive genetic testing for Lynch syndrome: the role of health professionals and families in decisions to decline.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 547, doi. 10.1007/s10689-018-0078-2
By:
- Kanga-Parabia, Anaita;
- Gaff, Clara;
- Flander, Louisa;
- Jenkins, Mark;
- Keogh, Louise A.
Publication type:
Article
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.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 545, doi. 10.1007/s10689-018-0077-3
By:
- Lythgoe, Mark P.;
- Malik, Salim S.;
- McPhail, Mark;
- Monahan, Kevin J.
Publication type:
Article
A retrospective review of 48 individuals, including 12 families, molecularly diagnosed with hereditary leiomyomatosis and renal cell cancer (HLRCC).
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 615, doi. 10.1007/s10689-018-0076-4
By:
- Bhola, Priya T.;
- Gilpin, Cathy;
- Smith, Amanda;
- Graham, Gail E.
Publication type:
Article
The first two confirmed sub-Saharan African families with germline TP53 mutations causing Li-Fraumeni syndrome.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 607, doi. 10.1007/s10689-018-0075-5
By:
- Macaulay, Shelley;
- Goodyear, Quintin Clive;
- Kruger, Mia;
- Chen, Wenlong;
- Essop, Fahmida;
- Krause, Amanda
Publication type:
Article
Commentary: PREMM5 threshold of 2.5% is recommended to improve identification of PMS2 carriers.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 567, doi. 10.1007/s10689-018-0074-6
By:
- Kastrinos, Fay;
- Uno, Hajime;
- Syngal, Sapna
Publication type:
Article
Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 601, doi. 10.1007/s10689-018-0073-7
By:
- Huq, A. J.;
- Walsh, M.;
- Rajagopalan, B.;
- Finlay, M.;
- Trainer, A. H.;
- Bonnet, F.;
- Sevenet, N.;
- Winship, I. M.
Publication type:
Article
APC mosaicism in a young woman with desmoid type fibromatosis and familial adenomatous polyposis.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 539, doi. 10.1007/s10689-018-0072-8
By:
- Stormorken, Astrid Tenden;
- Berg, Thomas;
- Norum, Ole-Jacob;
- Hølmebakk, Toto;
- Aaberg, Kristin;
- Steigen, Sonja E.;
- Grindedal, Eli Marie
Publication type:
Article
Risk management adherence following genetic testing for hereditary cancer syndromes: a Singaporean experience.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 621, doi. 10.1007/s10689-018-0071-9
By:
- Courtney, Eliza;
- Chin, Xin Wei;
- Yuen, Jeanette;
- Li, Shao-Tzu;
- Chen, Yanni;
- Allen, John Carson;
- Tan, Veronique;
- Lim, Geok Hoon;
- Ngeow, Joanne
Publication type:
Article
Clinical interpretation of pathogenic ATM and CHEK2 variants on multigene panel tests: navigating moderate risk.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 495, doi. 10.1007/s10689-018-0070-x
By:
- West, Allison H.;
- Blazer, Kathleen R.;
- Stoll, Jessica;
- Jones, Matthew;
- Weipert, Caroline M.;
- Nielsen, Sarah M.;
- Kupfer, Sonia S.;
- Weitzel, Jeffrey N.;
- Olopade, Olufunmilayo I.
Publication type:
Article
Letter to the editor.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 565, doi. 10.1007/s10689-018-0069-3
By:
- Anele, C. C.;
- Latchford, A.;
- Faiz, O.;
- Clark, S. K.
Publication type:
Article
Gene expression analysis in peripheral blood cells of patients with hereditary leiomyomatosis and renal cell cancer syndrome (HLRCC): identification of NRF2 pathway activation.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 587, doi. 10.1007/s10689-017-0068-9
By:
- Arenas Valencia, Carolina;
- Lopez Kleine, Liliana;
- Pinzon Velasco, Andres M.;
- Cardona Barreto, Andrea Y.;
- Arteaga Diaz, Clara E.
Publication type:
Article
SNP association study in PMS2-associated Lynch syndrome.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 507, doi. 10.1007/s10689-017-0061-3
By:
- ten Broeke, Sanne W.;
- Elsayed, Fadwa A.;
- Pagan, Lisa;
- Olderode-Berends, Maran J. W.;
- Garcia, Encarna Gomez;
- Gille, Hans J. P.;
- van Hest, Liselot P.;
- Letteboer, Tom G. W.;
- van der Kolk, Lizet E.;
- Mensenkamp, Arjen R.;
- van Os, Theo A.;
- Spruijt, Liesbeth;
- Redeker, Bert J. W.;
- Suerink, Manon;
- Vos, Yvonne J.;
- Wagner, Anja;
- Wijnen, Juul T.;
- Steyerberg, E. W.;
- Tops, Carli M. J.;
- van Wezel, Tom
Publication type:
Article
Adaptation of couples living with a high risk of breast/ovarian cancer and the association with risk-reducing surgery.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 485, doi. 10.1007/s10689-017-0065-z
By:
- Shapira, Rachel;
- Turbitt, Erin;
- Erby, Lori H.;
- Biesecker, Barbara B.;
- Klein, William M. P.;
- Hooker, Gillian W.
Publication type:
Article
Urological sequelae of desmoids associated with familial adenomatous polyposis.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 525, doi. 10.1007/s10689-017-0064-0
By:
- Walton, S. J.;
- Malietzis, G.;
- Clark, S. K.;
- Havranek, E.
Publication type:
Article
Feasibility of endoscopic resection using bipolar snare for nonampullary duodenal tumours in familial adenomatous polyposis patients.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 517, doi. 10.1007/s10689-017-0063-1
By:
- Inoki, Kazuya;
- Nakajima, Takeshi;
- Nonaka, Satoru;
- Abe, Seiichiro;
- Suzuki, Haruhisa;
- Yoshinaga, Shigetaka;
- Oda, Ichiro;
- Yamada, Masayoshi;
- Takatsu, Mizuki;
- Yoshida, Hiroshi;
- Taniguchi, Hirokazu;
- Sekine, Shigeki;
- Ohe, Yuichiro;
- Saito, Yutaka
Publication type:
Article
Metachronous colorectal cancer following segmental or extended colectomy in Lynch syndrome: a systematic review and meta-analysis.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 557, doi. 10.1007/s10689-017-0062-2
By:
- Malik, Salim S.;
- Lythgoe, Mark P.;
- McPhail, Mark;
- Monahan, Kevin J.
Publication type:
Article
Haplotype analysis suggest that the MLH1 c.2059C > T mutation is a Swedish founder mutation.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 531, doi. 10.1007/s10689-017-0067-x
By:
- von Salomé, Jenny;
- Liu, Tao;
- Keihäs, Markku;
- Morak, Moni;
- Holinski-Feder, Elke;
- Berry, Ian R.;
- Moilanen, Jukka S.;
- Baert-Desurmont, Stéphanie;
- Lindblom, Annika;
- Lagerstedt-Robinson, Kristina
Publication type:
Article
Mutations in context: implications of BRCA testing in diverse populations.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 471, doi. 10.1007/s10689-017-0038-2
By:
- Felix, Gabriela E. S.;
- Zheng, Yonglan;
- Olopade, Olufunmilayo I.
Publication type:
Article
Correlation of IL-31 gene polymorphisms with susceptibility and clinical recurrence of bladder cancer.
Published in:
Familial Cancer, 2018, v. 17, n. 4, p. 577, doi. 10.1007/s10689-017-0060-4
By:
- Li, Qin;
- Tang, Tielong;
- Zhang, Peng;
- Liu, Chenlu;
- Pu, Yan;
- Zhang, Yan;
- Song, Huizi;
- Wang, Yanyun;
- Song, Yaping;
- Su, Min;
- Zhou, Bin;
- Zhang, Lin
Publication type:
Article