Works matching IS 13899600 AND DT 2012 AND VI 11 AND IP 4

Results: 22

Cancer risks and immunohistochemical profiles linked to the Danish MLH1 Lynch syndrome founder mutation.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 579, doi. 10.1007/s10689-012-9552-4

By:

Therkildsen, Christina;
Isinger-Ekstrand, Anna;
Ladelund, Steen;
Nissen, Anja;
Rambech, Eva;
Bernstein, Inge;
Nilbert, Mef

Publication type:

Article

Multiple jejunal cancers resulting from combination of germline APC and MLH1 mutations.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 667, doi. 10.1007/s10689-012-9561-3

By:

Lindor, Noralane;
Smyrk, Tom;
Buehler, Sheila;
Gunawardena, Shanaka;
Thomas, Brittany;
Limburg, Paul;
Kirmani, Salman;
Thibodeau, Stephen

Publication type:

Article

Is the controversy on breast cancer as part of the Lynch-related tumor spectrum still open?

Published in:

2012

By:

Grandval, Philippe;
Barouk-Simonet, Emmanuelle;
Bronner, Myriam;
Buisine, Marie-Pierre;
Moretta, Jessica;
Tinat, Julie;
Olschwang, Sylviane

Publication type:

Letter

Consumer awareness and attitudes about insurance discrimination post enactment of the Genetic Information Nondiscrimination Act.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 637, doi. 10.1007/s10689-012-9564-0

By:

Allain, Dawn;
Friedman, Sue;
Senter, Leigha

Publication type:

Article

Hope-based intervention for individuals susceptible to colorectal cancer: a pilot study.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 545, doi. 10.1007/s10689-012-9545-3

By:

Ho, Samuel;
Ho, Judy;
Pau, Barbara;
Hui, Bryant;
Wong, Rosa;
Chu, Annie

Publication type:

Article

Advanced duodenal disease in familial adenomatous polyposis: how frequently should patients be followed up after successful therapy?

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 553, doi. 10.1007/s10689-012-9546-2

By:

Balmforth, Damian;
Phillips, Robin;
Clark, Susan

Publication type:

Article

Aberrant splicing caused by a MLH1 splice donor site mutation found in a young Japanese patient with Lynch syndrome.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 559, doi. 10.1007/s10689-012-9547-1

By:

Takahashi, Masanobu;
Furukawa, Yoichi;
Shimodaira, Hideki;
Sakayori, Masato;
Moriya, Takuya;
Moriya, Yoshihiro;
Nakamura, Yusuke;
Ishioka, Chikashi

Publication type:

Article

Bethesda criteria for microsatellite instability testing: impact on the detection of new cases of Lynch syndrome.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 571, doi. 10.1007/s10689-012-9550-6

By:

Serrano, Miguel;
Lage, Pedro;
Belga, Sara;
Filipe, Bruno;
Francisco, Inês;
Rodrigues, Paula;
Fonseca, Ricardo;
Chaves, Paula;
Claro, Isabel;
Albuquerque, Cristina;
Pereira, António

Publication type:

Article

Parent-of-origin in individuals with familial neurofibromatosis type 1 and optic pathway gliomas.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 653, doi. 10.1007/s10689-012-9549-z

By:

Johnson, K.;
Fisher, M.;
Listernick, R.;
North, K.;
Schorry, E.;
Viskochil, D.;
Weinstein, M.;
Rubin, J.;
Gutmann, D.

Publication type:

Article

Portuguese c.156_157insAlu BRCA2 founder mutation: gastrointestinal and tongue neoplasias may be part of the phenotype.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 657, doi. 10.1007/s10689-012-9551-5

By:

Moreira, Miguel;
Bobrovnitchaia, Irina;
Lima, Maria;
Santos, Anna;
Ramos, Jesus;
Souza, Kelly;
Peixoto, Ana;
Teixeira, Manuel;
Vargas, Fernando

Publication type:

Article

Two cases of nevoid basal cell carcinoma syndrome associated with meningioma caused by a PTCH1 or SUFU germline mutation.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 565, doi. 10.1007/s10689-012-9548-0

By:

Kijima, Chihiro;
Miyashita, Toshiyuki;
Suzuki, Maiko;
Oka, Hidehiro;
Fujii, Kiyotaka

Publication type:

Article

Heterozygote FANCD2 mutations associated with childhood T Cell ALL and testicular seminoma.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 661, doi. 10.1007/s10689-012-9553-3

By:

Smetsers, Stephanie;
Muter, Joanne;
Bristow, Claire;
Patel, Leena;
Chandler, Kate;
Bonney, Denise;
Wynn, Robert;
Whetton, Anthony;
Will, Andrew;
Rockx, Davy;
Joenje, Hans;
Strathdee, Gordon;
Shanks, Jonathan;
Klopocki, Eva;
Gille, Johan;
Dorsman, Josephine;
Meyer, Stefan

Publication type:

Article

Novel mutations of OGG1 base excision repair pathway gene in laryngeal cancer patients.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 587, doi. 10.1007/s10689-012-9554-2

By:

Mahjabeen, Ishrat;
Masood, Nosheen;
Baig, Ruqia;
Sabir, Maimoona;
Inayat, Uzma;
Malik, Faraz;
Kayani, Mahmood

Publication type:

Article

Routine TP53 testing for breast cancer under age 30: ready for prime time?

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 607, doi. 10.1007/s10689-012-9557-z

By:

McCuaig, Jeanna;
Armel, Susan;
Novokmet, Ana;
Ginsburg, Ophira;
Demsky, Rochelle;
Narod, Steven;
Malkin, David

Publication type:

Article

Sub-cellular localization analysis of MSH6 missense mutations does not reveal an overt MSH6 nuclear transport impairment.

Published in:

2012

By:

Belvederesi, Laura;
Bianchi, Francesca;
Loretelli, Cristian;
Bracci, Raffaella;
Cascinu, Stefano;
Cellerino, Riccardo

Publication type:

Letter

High frequency of BRCA1 founder mutations in Polish women with nonfamilial breast cancer.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 623, doi. 10.1007/s10689-012-9560-4

By:

Gaj, Pawel;
Kluska, Anna;
Nowakowska, Dorota;
Bałabas, Aneta;
Piątkowska, Magdalena;
Dabrowska, Michalina;
Niwińska, Anna;
Ostrowski, Jerzy

Publication type:

Article

No evidence for breast cancer susceptibility associated with variants of BRD7, a component of p53 and BRCA1 pathways.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 601, doi. 10.1007/s10689-012-9556-0

By:

Penkert, Judith;
Schlegelberger, Brigitte;
Steinemann, Doris;
Gadzicki, Dorothea

Publication type:

Article

Non-synonymous polymorphism (Gln261Arg) of 12-lipoxygenase in colorectal and thyroid cancers.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 615, doi. 10.1007/s10689-012-9559-x

By:

Prasad, Vidudala;
Padma, Kolli

Publication type:

Article

Low penetrance alleles as risk modifiers in familial and sporadic breast cancer.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 629, doi. 10.1007/s10689-012-9563-1

By:

Esteban Cardeñosa, Eva;
de Juan Jiménez, Inmaculada;
Palanca Suela, Sarai;
Chirivella González, Isabel;
Segura Huerta, Ángel;
Santaballa Beltran, Ana;
Casals El Busto, María;
Barragán González, Eva;
Fuster Lluch, Oscar;
Bermúdez Edo, José;
Bolufer Gilabert, Pascual

Publication type:

Article

Familial breast cancer: less emotional distress in adult daughters if they provide emotional support to their affected mother.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 645, doi. 10.1007/s10689-012-9566-y

By:

Vodermaier, Andrea;
Stanton, Annette

Publication type:

Article

Identification of a novel NBN truncating mutation in a family with hereditary prostate cancer.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 595, doi. 10.1007/s10689-012-9555-1

By:

Zuhlke, Kimberly;
Johnson, Anna;
Okoth, Linda;
Stoffel, Elena;
Robbins, Christiane;
Tembe, Waibov;
Salinas, Claudia;
Zheng, S.;
Xu, Jianfeng;
Carpten, John;
Lange, Ethan;
Isaacs, William;
Cooney, Kathleen

Publication type:

Article

Ovarian metastases of colorectal and duodenal cancer in familial adenomatous polyposis.

Published in:

Familial Cancer, 2012, v. 11, n. 4, p. 671, doi. 10.1007/s10689-012-9565-z

By:

Crobach, Stijn;
Wezel, Tom;
Vasen, Hans;
Morreau, Hans

Publication type:

Article