Works matching IS 13899600 AND DT 2012 AND VI 11 AND IP 1

Results: 19

Two novel mutations in hMLH1 gene in Iranian hereditary non-polyposis colorectal cancer patients.

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 13, doi. 10.1007/s10689-011-9478-2

By:

Shahmoradi, Somayeh;
Bidmeshkipour, Ali;
Salamian, Ahmad;
Emami, Mohammad;
Kazemi, Zahra;
Salehi, Mansoor

Publication type:

Article

A pre-visit tailored website enhances counselees' realistic expectations and knowledge and fulfils information needs for breast cancer genetic counselling.

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 85, doi. 10.1007/s10689-011-9479-1

By:

Albada, Akke;
Dulmen, Sandra;
Lindhout, Dick;
Bensing, Jozien;
Ausems, Margreet

Publication type:

Article

First degree relatives and familial aggregation of gastric cancer: who to choose for control in case-control studies?

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 137, doi. 10.1007/s10689-011-9488-0

By:

Marcos-Pinto, Ricardo;
Dinis-Ribeiro, Mário;
Carneiro, Fátima;
Machado, José;
Figueiredo, Ceu;
Reis, Celso;
Ferreira, José;
Areias, Jorge

Publication type:

Article

Non-cancer endpoints in BRCA1/2 carriers after risk-reducing salpingo-oophorectomy.

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 69, doi. 10.1007/s10689-011-9480-8

By:

Cohen, J.;
Chiel, L.;
Boghossian, L.;
Jones, M.;
Stopfer, J.;
Powers, J.;
Rebbeck, T.;
Nathanson, K.;
Domchek, S.

Publication type:

Article

BRCA1 and BRCA2 germline mutations in 85 Iranian breast cancer patients.

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 57, doi. 10.1007/s10689-011-9477-3

By:

Keshavarzi, Fatemeh;
Javadi, Gholam;
Zeinali, Sirous

Publication type:

Article

Uptake of a randomized breast cancer prevention trial comparing letrozole to placebo in BRCA1/ 2 mutations carriers: the LIBER trial.

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 77, doi. 10.1007/s10689-011-9484-4

By:

Pujol, Pascal;
Lasset, Christine;
Berthet, Pascaline;
Dugast, Catherine;
Delaloge, Suzette;
Fricker, Jean-Pierre;
Tennevet, Isabelle;
Chabbert-Buffet, Nathalie;
This, Pascale;
Baudry, Karen;
Lemonnier, Jerome;
Roca, Lise;
Mijonnet, Sylvie;
Gesta, Paul;
Chiesa, Jean;
Dreyfus, Helene;
Vennin, Philippe;
Delnatte, Capucine;
Bignon, Yves;
Lortholary, Alain

Publication type:

Article

The liver: another organ involved in Muir Torre syndrome?

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 7, doi. 10.1007/s10689-011-9450-1

By:

Morando, F.;
Alaibac, M.;
Romano, A.;
Cavallin, M.;
Piano, S.;
Pizzi, M.;
Mescoli, C.;
Pilati, P.;
Gatta, A.;
Angeli, P.

Publication type:

Article

Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy.

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 41, doi. 10.1007/s10689-011-9483-5

By:

Ghiorzo, P.;
Pensotti, V.;
Fornarini, G.;
Sciallero, S.;
Battistuzzi, L.;
Belli, F.;
Bonelli, L.;
Borgonovo, G.;
Bruno, W.;
Gozza, A.;
Gargiulo, S.;
Mastracci, L.;
Nasti, S.;
Palmieri, G.;
Papadia, F.;
Pastorino, L.;
Russo, A.;
Savarino, V.;
Varesco, L.;
Bernard, L.

Publication type:

Article

Implications for cancer genetics practice of pro-actively assessing family history in a General Practice cohort in North West London.

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 107, doi. 10.1007/s10689-011-9482-6

By:

Kohut, Kelly;
D'Mello, Lucia;
Bancroft, Elizabeth;
Thomas, Sarah;
Young, Mary-Anne;
Myhill, Kathryn;
Shanley, Susan;
Briggs, Brian;
Newman, Michelle;
Saraf, Ifthikhar;
Cox, Penny;
Scambler, Sarah;
Wagman, Lyndon;
Wyndham, Michael;
Eeles, Rosalind;
Ferris, Michelle

Publication type:

Article

Patient outcomes associated with group and individual genetic counseling formats.

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 97, doi. 10.1007/s10689-011-9486-2

By:

Rothwell, Erin;
Kohlmann, Wendy;
Jasperson, Kory;
Gammon, Amanda;
Wong, Bob;
Kinney, Anita

Publication type:

Article

Self-reported mammography use following BRCA1/2 genetic testing may be overestimated.

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 27, doi. 10.1007/s10689-011-9490-6

By:

Larouche, Geneviève;
Bouchard, Karine;
Chiquette, Jocelyne;
Desbiens, Christine;
Simard, Jacques;
Dorval, Michel

Publication type:

Article

Low prevalence of BRCA1 and BRCA2 mutations in the sporadic breast cancer of Spanish population.

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 49, doi. 10.1007/s10689-011-9481-7

By:

Juan Jiménez, Inmaculada;
Esteban Cardeñosa, Eva;
Palanca Suela, Sarai;
Barragán González, Eva;
Aznar Carretero, Ismael;
Munárriz Gandía, Blanca;
Santaballa Bertran, Ana;
Torregrosa Maicas, María;
Guillén Ponce, Carmen;
Sánchez Heras, Ana;
Bayón Lara, Ana;
Fuster Lluch, Oscar;
Bolufer Gilabert, Pascual

Publication type:

Article

Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors.

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 19, doi. 10.1007/s10689-011-9489-z

By:

Rahner, Nils;
Brockschmidt, Felix;
Steinke, Verena;
Kahl, Philip;
Becker, Tim;
Vasen, Hans;
Wijnen, Juul;
Tops, Carli;
Holinski-Feder, Elke;
Ligtenberg, Marjolijn;
Spruijt, Liesbeth;
Görgens, Heike;
Stemmler, Susanne;
Kloor, Matthias;
Dietmaier, Wolfgang;
Schumacher, Johannes;
Nöthen, Markus;
Propping, Peter

Publication type:

Article

Case report: a p.C618S RET proto-oncogene germline mutation in a large Chinese pedigree with familial medullary thyroid carcinoma.

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 131, doi. 10.1007/s10689-011-9487-1

By:

Qi, X.-P.;
Ying, R.-B.;
Ma, J.-M.;
Liu, W.-T.;
Du, Z.-F.;
Fei, J.;
Yang, C.-P.;
Song, Q.-Z.;
Jin, H.-Y.;
Chen, Z.-G.;
Han, J.-S.;
Wang, J.-Q.;
Chen, X.-L.;
Zhao, Y.;
Lu, J.-J.;
Zhang, X.-N.

Publication type:

Article

Hereditary leiomyomatosis and renal cell cancer presenting as metastatic kidney cancer at 18 years of age: implications for surveillance.

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 123, doi. 10.1007/s10689-011-9491-5

By:

Spaendonck-Zwarts, Karin;
Badeloe, Sadhanna;
Oosting, Sjoukje;
Hovenga, Sjoerd;
Semmelink, Harry;
Moorselaar, R.;
Waesberghe, Jan;
Mensenkamp, Arjen;
Menko, Fred

Publication type:

Article

A state-wide population-based program for detection of lynch syndrome based upon immunohistochemical and molecular testing of colorectal tumours.

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 1, doi. 10.1007/s10689-011-9494-2

By:

Schofield, Lyn;
Grieu, Fabienne;
Goldblatt, Jack;
Amanuel, Benhur;
Iacopetta, Barry

Publication type:

Article

Increased incidence of childhood, prostate and breast cancers in relatives of childhood cancer patients.

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 145, doi. 10.1007/s10689-011-9493-3

By:

Magnusson, Susanne;
Wiebe, Thomas;
Kristoffersson, Ulf;
Jernström, Helena;
Olsson, Håkan

Publication type:

Article

Evaluation of the BOADICEA risk assessment model in women with a family history of breast cancer.

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 33, doi. 10.1007/s10689-011-9495-1

By:

Ståhlbom, Anne;
Johansson, Hemming;
Liljegren, Annelie;
Wachenfeldt, Anna;
Arver, Brita

Publication type:

Article

Familial renal cancer as an indicator of hereditary leiomyomatosis and renal cell cancer syndrome.

Published in:

Familial Cancer, 2012, v. 11, n. 1, p. 115, doi. 10.1007/s10689-011-9485-3

By:

Raymond, Victoria;
Herron, Casey;
Giordano, Thomas;
Gruber, Stephen

Publication type:

Article