Works matching IS 13899600 AND DT 2018 AND VI 17 AND IP 3

Results: 20

Excluding Lynch syndrome in a female patient with metachronous DNA mismatch repair deficient colon- and ovarian cancer.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 415, doi. 10.1007/s10689-017-0055-1

By:

Crobach, Stijn;
Jansen, Anne M. L.;
Ligtenberg, Marjolein J. L.;
Koopmans, Marije;
Nielsen, Maartje;
Hes, Frederik J.;
Wijnen, Juul T.;
Dinjens, Winand N. M.;
van Wezel, Tom;
Morreau, Hans

Publication type:

Article

Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 403, doi. 10.1007/s10689-017-0053-3

By:

Lynch, Henry T.;
Lanspa, Stephen;
Shaw, Trudy;
Casey, Murray Joseph;
Rendell, Marc;
Stacey, Mark;
Townley, Theresa;
Snyder, Carrie;
Hitchins, Megan;
Bailey-Wilson, Joan

Publication type:

Article

Universal determination of microsatellite instability using BAT26 as a single marker in an Argentine colorectal cancer cohort.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 395, doi. 10.1007/s10689-017-0052-4

By:

González, María Laura;
Causada-Calo, Natalia;
Santino, Juan Pablo;
Dominguez-Valentin, Mev;
Ferro, Fabiana Alejandra;
Sammartino, Inés;
Kalfayan, Pablo Germán;
Verzura, Maria Alicia;
Piñero, Tamara Alejandra;
Cajal, Andrea Romina;
Pavicic, Walter;
Vaccaro, Carlos

Publication type:

Article

Information and support needs of young women regarding breast cancer risk and genetic testing: adapting effective interventions for a novel population.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 351, doi. 10.1007/s10689-017-0059-x

By:

O’Neill, Suzanne C.;
Evans, Chalanda;
Hamilton, Rebekah J.;
Peshkin, Beth N.;
Isaacs, Claudine;
Friedman, Sue;
Tercyak, Kenneth P.

Publication type:

Article

Genotype phenotype correlation in Asian Indian von Hippel-Lindau (VHL) syndrome patients with pheochromocytoma/paraganglioma.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 441, doi. 10.1007/s10689-017-0058-y

By:

Lomte, Nilesh;
Kumar, Sanjeet;
Sarathi, Vijaya;
Pandit, Reshma;
Goroshi, Manjunath;
Jadhav, Swati;
Lila, Anurag R.;
Bandgar, Tushar;
Shah, Nalini S.

Publication type:

Article

Association between miR-146a rs2910164 polymorphism and specific cancer susceptibility: an updated meta-analysis.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 459, doi. 10.1007/s10689-017-0056-0

By:

Hao, Xia;
Xia, Lingzi;
Qu, Ruoyi;
Yang, Xianglin;
Jiang, Min;
Zhou, Baosen

Publication type:

Article

Corrections to: Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 469, doi. 10.1007/s10689-017-0051-5

By:

Brédart, Anne;
Kop, Jean‑Luc;
Antoniou, Antonis C.;
Cunningham, Alex P.;
De Pauw, Antoine;
Tischkowitz, Marc;
Ehrencrona, Hans;
Dolbeault, Sylvie;
Robieux, Léonore;
Rhiem, Kerstin;
Easton, Douglas F.;
Devilee, Peter;
Stoppa‑Lyonnet, Dominique;
Schmutlzer, Rita

Publication type:

Article

Germline variant in MSX1 identified in a Dutch family with clustering of Barrett’s esophagus and esophageal adenocarcinoma.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 435, doi. 10.1007/s10689-017-0054-2

By:

van Nistelrooij, A. M. J.;
van Marion, R.;
van Ijcken, W. F. J.;
de Klein, A.;
Wagner, A.;
Biermann, K.;
Spaander, M. C. W.;
van Lanschot, J. J. B.;
Dinjens, W. N. M.;
Wijnhoven, B. P. L.

Publication type:

Article

Targeted massively parallel sequencing characterises the mutation spectrum of PALB2 in breast and ovarian cancer cases from Poland and Ukraine.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 345, doi. 10.1007/s10689-017-0050-6

By:

Myszka, Aleksander;
Nguyen-Dumont, Tu;
Karpinski, Pawel;
Sasiadek, Maria M.;
Akopyan, Hayane;
Hammet, Fleur;
Tsimiklis, Helen;
Park, Daniel J.;
Pope, Bernard J.;
Slezak, Ryszard;
Kitsera, Nataliya;
Siekierzynska, Aleksandra;
Southey, Melissa C.

Publication type:

Article

Cost-effectiveness evaluation of pre-counseling telephone interviews before face-to-face genetic counseling in cancer genetics.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 451, doi. 10.1007/s10689-017-0049-z

By:

Collet, Gaëlle;
Parodi, Nathalie;
Cassinari, Kevin;
Neviere, Zoe;
Cohen, Fanny;
Gasnier, Céline;
Brahimi, Afane;
Lecoquierre, François;
Thery, Jean-Christophe;
Tennevet, Isabelle;
Lacaze, Elodie;
Berthet, Pascaline;
Frebourg, Thierry

Publication type:

Article

Penetrance of a rare familial mutation predisposing to papillary thyroid cancer.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 431, doi. 10.1007/s10689-017-0048-0

By:

Saporito, Donika;
Brock, Pamela;
Hampel, Heather;
Sipos, Jennifer;
Fernandez, Soledad;
Liyanarachchi, Sandya;
de la Chapelle, Albert;
Nagy, Rebecca

Publication type:

Article

Cancer risk management in Tasmanian women with BRCA1 and BRCA2 mutations.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 333, doi. 10.1007/s10689-017-0047-1

By:

Kearton, Stephanie;
Wills, Karen;
Bunting, Michael;
Blomfield, Penny;
James, Paul A.;
Burke, Jo

Publication type:

Article

Family history influences the tumor characteristics and prognosis of breast cancers developing during postmenopausal hormone therapy.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 321, doi. 10.1007/s10689-017-0046-2

By:

Fagerholm, Rainer;
Faltinova, Maria;
Aaltonen, Kirsi;
Aittomäki, Kristiina;
Heikkilä, Päivi;
Halttunen-Nieminen, Mervi;
Nevanlinna, Heli;
Blomqvist, Carl

Publication type:

Article

Germline mutations in lung cancer and personalized medicine.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 429, doi. 10.1007/s10689-017-0044-4

By:

Cetta, Francesco;
Renieri, Alessandra;
Frullanti, Elisa

Publication type:

Article

Screening for germline mutations in mismatch repair genes in patients with Lynch syndrome by next generation sequencing.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 387, doi. 10.1007/s10689-017-0043-5

By:

Soares, Barbara Luísa;
Brant, Ayslan Castro;
Gomes, Renan;
Pastor, Tatiane;
Schneider, Naye Balzan;
Ribeiro-dos-Santos, Ândrea;
de Assumpção, Paulo Pimentel;
Achatz, Maria Isabel W.;
Ashton-Prolla, Patrícia;
Moreira, Miguel Angelo Martins

Publication type:

Article

Ectopic, retroperitoneal adrenocortical carcinoma in the setting of Lynch syndrome.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 381, doi. 10.1007/s10689-017-0042-6

By:

Wright, Jesse P.;
Montgomery, Kathleen W.;
Tierney, Joshua;
Gilbert, Jill;
Solórzano, Carmen C.;
Idrees, Kamran

Publication type:

Article

Evaluation of an online family history tool for identifying hereditary and familial colorectal cancer.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 371, doi. 10.1007/s10689-017-0041-7

By:

Kallenberg, F. G. J.;
Aalfs, C. M.;
The, F. O.;
Wientjes, C. A.;
Depla, A. C.;
Mundt, M. W.;
Bossuyt, P. M. M.;
Dekker, E.

Publication type:

Article

Evaluation of current prediction models for Lynch syndrome: updating the PREMM5 model to identify PMS2 mutation carriers.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 361, doi. 10.1007/s10689-017-0039-1

By:

Goverde, A.;
Spaander, M. C. W.;
Nieboer, D.;
van den Ouweland, A. M. W.;
Dinjens, W. N. M.;
Dubbink, H. J.;
Tops, C. J.;
ten Broeke, S. W.;
Bruno, M. J.;
Hofstra, R. M. W.;
Steyerberg, E. W.;
Wagner, A.

Publication type:

Article

An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 421, doi. 10.1007/s10689-017-0037-3

By:

Daniell, Julian;
Plazzer, John-Paul;
Perera, Anuradha;
Macrae, Finlay

Publication type:

Article

Increased access to TP53 analysis through breast cancer multi-gene panels: clinical considerations.

Published in:

Familial Cancer, 2018, v. 17, n. 3, p. 317, doi. 10.1007/s10689-017-0020-z

By:

Azzollini, Jacopo;
Mariani, Milena;
Peissel, Bernard;
Manoukian, Siranoush

Publication type:

Article