Works matching IS 13899600 AND DT 2014 AND VI 13 AND IP 1

Results: 16

Endometrial tumour BRAF mutations and MLH1 promoter methylation as predictors of germline mismatch repair gene mutation status: a literature review.

Published in:

Familial Cancer, 2014, v. 13, n. 1, p. 1, doi. 10.1007/s10689-013-9671-6

By:

Metcalf, Alexander;
Spurdle, Amanda

Publication type:

Article

Genetic variation at 8q24, family history of cancer, and upper gastrointestinal cancers in a Chinese population.

Published in:

Familial Cancer, 2014, v. 13, n. 1, p. 45, doi. 10.1007/s10689-013-9673-4

By:

Tarleton, Heather;
Chang, Shen-Chih;
Park, Sungshim;
Cai, Lin;
Ding, Baoguo;
He, Na;
Hussain, Shehnaz;
Jiang, Qingwu;
Mu, Li-Na;
Rao, Jianyu;
Wang, Hua;
You, Nai-Chieh;
Yu, Shun-Zhang;
Zhao, Jin-Kou;
Zhang, Zuo-Feng

Publication type:

Article

Lack of association between let-7 binding site polymorphism rs712 and risk of nasopharyngeal carcinoma.

Published in:

Familial Cancer, 2014, v. 13, n. 1, p. 93, doi. 10.1007/s10689-013-9681-4

By:

Pan, Xin-Min;
Jia, Jing;
Guo, Xiao-Min;
Li, Zhao-Hui;
Zhang, Zhen;
Qin, Hao-Jie;
Xu, Guo-Hui;
Gao, Lin-Bo

Publication type:

Article

Lynch Syndrome in high risk Ashkenazi Jews in Israel.

Published in:

Familial Cancer, 2014, v. 13, n. 1, p. 65, doi. 10.1007/s10689-013-9675-2

By:

Goldberg, Yael;
Kedar, Inbal;
Kariiv, Revital;
Halpern, Naama;
Plesser, Morasha;
Hubert, Ayala;
Kaduri, Luna;
Sagi, Michal;
Lerer, Israela;
Abeliovich, Dvorah;
Hamburger, Tamar;
Nissan, Aviram;
Goldshmidt, Hanoch;
Solar, Irit;
Geva, Ravit;
Strul, Hana;
Rosner, Guy;
Baris, Hagit;
Levi, Zohar;
Peretz, Tamar

Publication type:

Article

Diversity of the clinical presentation of the MMR gene biallelic mutations.

Published in:

Familial Cancer, 2014, v. 13, n. 1, p. 131, doi. 10.1007/s10689-013-9676-1

By:

Bougeard, Gaëlle;
Olivier-Faivre, Laurence;
Baert-Desurmont, Stéphanie;
Tinat, Julie;
Martin, Cosette;
Bouvignies, Emilie;
Vasseur, Stéphanie;
Huet, Frédéric;
Couillault, Gérard;
Vabres, Pierre;
Le Pessot, Florence;
Chapusot, Caroline;
Malka, David;
Bressac-de Paillerets, Brigitte;
Tosi, Mario;
Frebourg, Thierry

Publication type:

Article

Cancer risk and overall survival in mismatch repair proficient hereditary non-polyposis colorectal cancer, Lynch syndrome and sporadic colorectal cancer.

Published in:

Familial Cancer, 2014, v. 13, n. 1, p. 109, doi. 10.1007/s10689-013-9683-2

By:

Garre, Pilar;
Martín, Lorena;
Bando, Inmaculada;
Tosar, Alicia;
Llovet, Patricia;
Sanz, Julián;
Romero, Atocha;
Hoya, Miguel;
Díaz-Rubio, Eduardo;
Caldés, Trinidad

Publication type:

Article

Mammographic surveillance in women aged 35-39 at enhanced familial risk of breast cancer (FH02).

Published in:

Familial Cancer, 2014, v. 13, n. 1, p. 13, doi. 10.1007/s10689-013-9661-8

By:

Evans, D.;
Thomas, S.;
Caunt, J.;
Roberts, L.;
Howell, A.;
Wilson, M.;
Fox, R.;
Sibbering, D.;
Moss, S.;
Wallis, M.;
Eccles, D.;
Duffy, S.

Publication type:

Article

No evidence of genetic anticipation in a large family with Lynch syndrome.

Published in:

Familial Cancer, 2014, v. 13, n. 1, p. 29, doi. 10.1007/s10689-013-9669-0

By:

Stupart, D.;
Goldberg, P.;
Algar, U.;
Vorster, A.;
Ramesar, R.

Publication type:

Article

The prevalence of small intestinal polyps in patients with familial adenomatous polyposis: a prospective capsule endoscopy study.

Published in:

Familial Cancer, 2014, v. 13, n. 1, p. 23, doi. 10.1007/s10689-013-9668-1

By:

Yamada, Atsuo;
Watabe, Hirotsugu;
Iwama, Takeo;
Obi, Shuntaro;
Omata, Masao;
Koike, Kazuhiko

Publication type:

Article

Illness perceptions, risk perception and worry in SDH mutation carriers.

Published in:

Familial Cancer, 2014, v. 13, n. 1, p. 83, doi. 10.1007/s10689-013-9680-5

By:

Hulsteijn, L.;
Kaptein, A.;
Louisse, A.;
Biermasz, N.;
Smit, J.;
Corssmit, E.

Publication type:

Article

Cancer risk and genotype-phenotype correlations in PTEN hamartoma tumor syndrome.

Published in:

Familial Cancer, 2014, v. 13, n. 1, p. 57, doi. 10.1007/s10689-013-9674-3

By:

Nieuwenhuis, Marry;
Kets, C.;
Murphy-Ryan, Maureen;
Yntema, Helger;
Evans, D.;
Colas, Chrystelle;
Møller, Pal;
Hes, Frederik;
Hodgson, Shirley;
Olderode-Berends, Maran;
Aretz, Stefan;
Heinimann, Karl;
Gómez García, Encarna;
Douglas, Fiona;
Spigelman, Allan;
Timshel, Susanne;
Lindor, Noralane;
Vasen, Hans

Publication type:

Article

Does and should breast cancer genetic counselling include lifestyle advice?

Published in:

Familial Cancer, 2014, v. 13, n. 1, p. 35, doi. 10.1007/s10689-013-9672-5

By:

Albada, Akke;
Vernooij, Madelèn;
Osch, Liesbeth;
Pijpe, Anouk;
Dulmen, Sandra;
Ausems, Margreet

Publication type:

Article

Reflex testing for Lynch syndrome: If we build it, will they come? Lessons learned from the uptake of clinical genetics services by individuals with newly diagnosed colorectal cancer (CRC).

Published in:

Familial Cancer, 2014, v. 13, n. 1, p. 75, doi. 10.1007/s10689-013-9677-0

By:

Tomiak, E.;
Samson, A.;
Spector, N.;
Mackey, M.;
Gilpin, C.;
Smith, E.;
Jonker, D.;
Allanson, J.;
Asmis, T.

Publication type:

Article

The MDM2 285G-309G haplotype is associated with an earlier age of tumour onset in patients with Li-Fraumeni syndrome.

Published in:

Familial Cancer, 2014, v. 13, n. 1, p. 127, doi. 10.1007/s10689-013-9667-2

By:

Renaux-Petel, Mariette;
Sesboüé, Richard;
Baert-Desurmont, Stéphanie;
Vasseur, Stéphanie;
Fourneaux, Steeve;
Bessenay, Emilie;
Frébourg, Thierry;
Bougeard, Gaëlle

Publication type:

Article

MAX mutations status in Swedish patients with pheochromocytoma and paraganglioma tumours.

Published in:

Familial Cancer, 2014, v. 13, n. 1, p. 121, doi. 10.1007/s10689-013-9666-3

By:

Crona, Joakim;
Maharjan, Rajani;
Delgado Verdugo, Alberto;
Stålberg, Peter;
Granberg, Dan;
Hellman, Per;
Björklund, Peyman

Publication type:

Article

Impact of breast cancer family history on tumor detection and tumor size in women newly-diagnosed with invasive breast cancer.

Published in:

Familial Cancer, 2014, v. 13, n. 1, p. 99, doi. 10.1007/s10689-013-9682-3

By:

Schwab, Fabienne;
Bürki, Nicole;
Huang, Dorothy;
Heinzelmann-Schwarz, Viola;
Schmid, Seraina;
Vetter, Marcus;
Schötzau, Andreas;
Güth, Uwe

Publication type:

Article