Works matching IS 13899600 AND DT 2010 AND VI 9 AND IP 2

Results: 21

No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndrome.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 245, doi. 10.1007/s10689-009-9312-2

By:

Vahteristo, Pia;
Koski, Taru;
Näätsaari, Laura;
Kiuru, Maija;
Karhu, Auli;
Herva, Riitta;
Sallinen, Satu-Leena;
Vierimaa, Outi;
Björck, Erik;
Richard, Stéphane;
Gardie, Betty;
Bessis, Didier;
Glabeke, Emmanuel;
Blanco, Ignacio;
Houlston, Richard;
Senter, Leigha;
Hietala, Marja;
Aittomäki, Kristiina;
Aaltonen, Lauri;
Launonen, Virpi

Publication type:

Article

Retrospective comparison of patient outcomes after in-person and telephone results disclosure counseling for BRCA1/2 genetic testing.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 203, doi. 10.1007/s10689-009-9303-3

By:

Doughty Rice, Courtney;
Ruschman, Jennifer;
Martin, Lisa;
Manders, Jennifer;
Miller, Erin

Publication type:

Article

Heterogeneous prevalence of recurrent BRCA1 and BRCA2 mutations in Spain according to the geographical area: implications for genetic testing.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 187, doi. 10.1007/s10689-009-9301-5

By:

Diez, Orland;
Gutiérrez-Enríquez, Sara;
Balmaña, Judith

Publication type:

Article

Erratum to: FAP-associated desmoid invasiveness correlates with in vitro resistance to doxorubicin.

Published in:

2010

By:

Joyner, David;
Trang, Sylvia;
Aboulafia, Albert;
Damron, Timothy;
Randall, R.

Publication type:

Correction Notice

Efficiency of BRCAPRO and Myriad II mutation probability thresholds versus cancer history criteria alone for BRCA1/ 2 mutation detection.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 193, doi. 10.1007/s10689-009-9305-1

By:

Harssel, J.;
Roozendaal, C.;
Detisch, Y.;
Brandão, R.;
Paulussen, A.;
Zeegers, M.;
Blok, M.;
Gómez García, E.

Publication type:

Article

Selection of patients with germline MLH1 mutated Lynch syndrome by determination of MLH1 methylation and BRAF mutation.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 167, doi. 10.1007/s10689-009-9302-4

By:

Bouzourene, Hanifa;
Hutter, Pierre;
Losi, Lorena;
Martin, Patricia;
Benhattar, Jean

Publication type:

Article

Serum antibodies against frameshift peptides in microsatellite unstable colorectal cancer patients with Lynch syndrome.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 173, doi. 10.1007/s10689-009-9307-z

By:

Reuschenbach, Miriam;
Kloor, Matthias;
Morak, Monika;
Wentzensen, Nicolas;
Germann, Anja;
Garbe, Yvette;
Tariverdian, Mirjam;
Findeisen, Peter;
Neumaier, Michael;
Holinski-Feder, Elke;
Knebel Doeberitz, Magnus

Publication type:

Article

Evolving perspectives on genetic discrimination in health insurance among health care providers.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 253, doi. 10.1007/s10689-009-9308-y

By:

Huizenga, Carin;
Lowstuter, Katrina;
Banks, Kimberly;
Lagos, Veronica;
Vandergon, Virginia;
Weitzel, Jeffrey

Publication type:

Article

Female BRCA mutation carriers with a preference for prophylactic mastectomy are more likely to participate an educational-support group and to proceed with the preferred intervention within 2 years.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 213, doi. 10.1007/s10689-009-9311-3

By:

Landsbergen, Karin;
Prins, Judith;
Kamm, Yvonne;
Brunner, Han;
Hoogerbrugge, Nicoline

Publication type:

Article

Hereditary leiomyomatosis and renal cell carcinoma: very early diagnosis of renal cancer in a paediatric patient.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 239, doi. 10.1007/s10689-009-9306-0

By:

Alrashdi, Ismail;
Levine, Samantha;
Paterson, Joan;
Saxena, Rohit;
Patel, Soonie;
Depani, Sarita;
Hargrave, Darren;
Pritchard-Jones, Kathy;
Hodgson, Shirley

Publication type:

Article

Evaluating Lynch syndrome in very early onset colorectal cancer probands without apparent polyposis.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 99, doi. 10.1007/s10689-009-9290-4

By:

Jasperson, Kory;
Vu, Thuy;
Schwab, Angela;
Neklason, Deborah;
Rodriguez-Bigas, Miguel;
Burt, Randall;
Weitzel, Jeffrey

Publication type:

Article

Clinical and histomolecular endometrial tumor characterization of patients at-risk for Lynch syndrome in South of Brazil.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 131, doi. 10.1007/s10689-009-9297-x

By:

Cossio, Silvia;
Koehler-Santos, Patricia;
Pessini, Suzana;
Mónego, Heleuza;
Edelweiss, Maria;
Meurer, Luise;
Errami, Abdellatif;
Coffa, Jordy;
Bock, Hugo;
Saraiva-Pereira, Maria;
Ashton-Prolla, Patricia;
Prolla, João

Publication type:

Article

Recommendations to improve identification of hereditary and familial colorectal cancer in Europe.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 109, doi. 10.1007/s10689-009-9291-3

By:

Vasen, H.;
Möslein, G.;
Alonso, A.;
Aretz, S.;
Bernstein, I.;
Bertario, L.;
Blanco, I.;
Bulow, S.;
Burn, J.;
Capella, G.;
Colas, C.;
Engel, C.;
Frayling, I.;
Rahner, N.;
Hes, F.;
Hodgson, S.;
Mecklin, J.-P.;
Møller, P.;
Myrhøj, T.;
Nagengast, F.

Publication type:

Article

A PALB2 germline mutation associated with hereditary breast cancer in Italy.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 181, doi. 10.1007/s10689-009-9295-z

By:

Papi, Laura;
Putignano, Anna;
Congregati, Caterina;
Piaceri, Irene;
Zanna, Ines;
Sera, Francesco;
Morrone, Doralba;
Genuardi, Maurizio;
Palli, Domenico

Publication type:

Article

Mutation analysis of the APC gene in Taiwanese FAP families: low incidence of APC germline mutation in a distinct subgroup of FAP families.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 117, doi. 10.1007/s10689-009-9292-2

By:

Chiang, J.;
Chen, H.;
Tang, R.;
Chen, J.;
Changchien, C.;
Hsieh, P.;
Wang, J.

Publication type:

Article

Outcomes of nasopharyngeal carcinoma screening for high risk family members in Hong Kong.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 221, doi. 10.1007/s10689-009-9296-y

By:

Ng, Wai;
Choi, Cheuk;
Lee, Michael;
Law, Lai;
Yau, Tsz;
Lee, Anne

Publication type:

Article

Frequent alterations of the PI3K/AKT/mTOR pathways in hereditary nonpolyposis colorectal cancer.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 125, doi. 10.1007/s10689-009-9293-1

By:

Ekstrand, Anna;
Jönsson, Mats;
Lindblom, Annika;
Borg, Åke;
Nilbert, Mef

Publication type:

Article

An Ashkenazi founder mutation in the MSH6 gene leading to HNPCC.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 141, doi. 10.1007/s10689-009-9298-9

By:

Goldberg, Yael;
Porat, Rinnat;
Kedar, Inbal;
Shochat, Chen;
Galinsky, Daliah;
Hamburger, Tamar;
Hubert, Ayala;
Strul, Hana;
Kariiv, Revital;
Ben-Avi, Liat;
Savion, Moran;
Pikarsky, Eli;
Abeliovich, Dvorah;
Bercovich, Dani;
Lerer, Israela;
Peretz, Tamar

Publication type:

Article

Heredity, diet and lifestyle as determining risk factors for the esophageal cancer on Nanao Island in Southern China.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 229, doi. 10.1007/s10689-009-9300-6

By:

Liu, Min;
Su, Min;
Tian, Dong-Ping;
Zhang, Guo-Hong;
Yang, He-Lin;
Gao, Yu-Xia

Publication type:

Article

Biallelic MYH germline mutations as cause of Muir-Torre syndrome.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 151, doi. 10.1007/s10689-009-9309-x

By:

Guillén-Ponce, Carmen;
Castillejo, Adela;
Barberá, Víctor;
Pascual-Ramírez, J.;
Andrada, Encarnación;
Castillejo, M.;
Guarinós, Carla;
Molina-Garrido, M.;
Carrato, Alfredo;
Soto, J.

Publication type:

Article

Mismatch repair protein expression and colorectal cancer in Hispanics from Puerto Rico.

Published in:

Familial Cancer, 2010, v. 9, n. 2, p. 155, doi. 10.1007/s10689-009-9310-4

By:

De Jesus-Monge, Wilfredo;
Gonzalez-Keelan, Carmen;
Zhao, Ronghua;
Hamilton, Stanley;
Rodriguez-Bigas, Miguel;
Cruz-Correa, Marcia

Publication type:

Article