Works matching IS 13899600 AND DT 2019 AND VI 18 AND IP 3

Results: 12

Targeted next generation sequencing screening of Lynch syndrome in Tunisian population.

Published in:

Familial Cancer, 2019, v. 18, n. 3, p. 343, doi. 10.1007/s10689-019-00130-y

By:

Ben Sghaier, Rihab;
Jansen, Anne Maria Lucia;
Bdioui, Ahlem;
Van Wezel, Tom;
ksiaa, Mehdi;
Elgolli, Lamia;
Ben Fatma, Leila;
Ben Ahmed, Slim;
Azzouz, Mohamed Msaddak;
Hellara, Olfa;
Elghali, Amine;
Darbel, Fathi;
Skandrani, Karim;
Mokkni, Moncef;
Gdissa, Ameni;
Ltaief, Rached;
Saad, Ali;
Hmila, Fahmi;
Gribaa, Moez;
Morreau, Hans

Publication type:

Article

Endoscopic full thickness resection for early colon cancer in Lynch syndrome.

Published in:

Familial Cancer, 2019, v. 18, n. 3, p. 349, doi. 10.1007/s10689-019-00132-w

By:

Langers, Alexandra M. J.;
Boonstra, Jurjen J.;
Hardwick, James C. H.;
van der Kraan, Jolein;
Farina Sarasqueta, Arantza;
Vasen, Hans F.A.

Publication type:

Article

The incidence of consecutive manifestations in Von Hippel-Lindau disease.

Published in:

Familial Cancer, 2019, v. 18, n. 3, p. 369, doi. 10.1007/s10689-019-00131-x

By:

van der Horst-Schrivers, Anouk N. A.;
Sluiter, Wim J.;
Kruizinga, Roeliene C.;
van Leeuwaarde, Rachel S.;
Giles, Rachel;
Olderode-Berends, Maran J. W.;
Links, Thera P.

Publication type:

Article

Implication of DNA repair genes in Lynch-like syndrome.

Published in:

Familial Cancer, 2019, v. 18, n. 3, p. 331, doi. 10.1007/s10689-019-00128-6

By:

Xicola, Rosa M.;
Clark, Julia R.;
Carroll, Timothy;
Alvikas, Jurgis;
Marwaha, Priti;
Regan, Maureen R.;
Lopez-Giraldez, Francesc;
Choi, Jungmin;
Emmadi, Rajyasree;
Alagiozian-Angelova, Victoria;
Kupfer, Sonia S.;
Ellis, Nathan A.;
Llor, Xavier

Publication type:

Article

Genetic counseling referral for ovarian cancer patients: a call to action.

Published in:

Familial Cancer, 2019, v. 18, n. 3, p. 303, doi. 10.1007/s10689-019-00129-5

By:

Garcia, Christine;
Harrison, Kara;
Ring, Kari L.;
Sullivan, Mackenzie W.;
Rauh, Lisa A.;
Modesitt, Susan C.

Publication type:

Article

Hereditary gastric cancer: what's new? Update 2013–2018.

Published in:

Familial Cancer, 2019, v. 18, n. 3, p. 363, doi. 10.1007/s10689-019-00127-7

By:

van der Post, Rachel S.;
Oliveira, Carla;
Guilford, Parry;
Carneiro, Fátima

Publication type:

Article

Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care Setting.

Published in:

Familial Cancer, 2019, v. 18, n. 3, p. 317, doi. 10.1007/s10689-019-00123-x

By:

Clarke, Elizabeth V.;
Muessig, Kristin R.;
Zepp, Jamilyn;
Hunter, Jessica E.;
Syngal, Sapna;
Acheson, Louise S.;
Wiesner, Georgia L.;
Peterson, Susan K.;
Bergen, Kellene M.;
Shuster, Elizabeth;
Davis, James V.;
Schneider, Jennifer L.;
Kauffman, Tia L.;
Gilmore, Marian J.;
Reiss, Jacob A.;
Rope, Alan F.;
Cook, Jennifer E.;
Goddard, Katrina A. B.

Publication type:

Article

Pediatric craniopharyngioma in association with familial adenomatous polyposis.

Published in:

Familial Cancer, 2019, v. 18, n. 3, p. 327, doi. 10.1007/s10689-019-00126-8

By:

Dahl, Nathan A.;
Pratt, Drew;
Camelo-Piragua, Sandra;
Kumar-Sinha, Chandan;
Mody, Rajen J.;
Septer, Seth;
Hankinson, Todd C.;
Chinnaiyan, Arul M.;
Koschmann, Carl;
Hoffman, Lindsey

Publication type:

Article

Progress report: familial pancreatic cancer.

Published in:

Familial Cancer, 2019, v. 18, n. 3, p. 359, doi. 10.1007/s10689-019-00125-9

By:

Mintziras, Ioannis;
Bartsch, Detlef K.

Publication type:

Article

Mutated SON putatively causes a cancer syndrome comprising high-risk medulloblastoma combined with café-au-lait spots.

Published in:

Familial Cancer, 2019, v. 18, n. 3, p. 353, doi. 10.1007/s10689-019-00121-z

By:

Chiu, Celine;
Loth, Stefanie;
Kuhlen, Michaela;
Ginzel, Sebastian;
Schaper, Jörg;
Rosenbaum, Thorsten;
Pietsch, Torsten;
Borkhardt, Arndt;
Hoell, Jessica I.

Publication type:

Article

Moving into the mainstream: healthcare professionals' views of implementing treatment focussed genetic testing in breast cancer care.

Published in:

Familial Cancer, 2019, v. 18, n. 3, p. 293, doi. 10.1007/s10689-019-00122-y

By:

Hallowell, Nina;
Wright, S.;
Stirling, D.;
Gourley, C.;
Young, O.;
Porteous, M.

Publication type:

Article

Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene.

Published in:

Familial Cancer, 2019, v. 18, n. 3, p. 311, doi. 10.1007/s10689-019-00120-0

By:

Beard, Catherine;
Purvis, Rebecca;
Winship, Ingrid M.;
Macrae, Finlay A.;
Buchanan, Daniel D.

Publication type:

Article