Works matching IS 13899600 AND DT 2014 AND VI 13 AND IP 3

Results: 23

A family history questionnaire improves detection of women at risk for hereditary gynecologic cancer: a pilot study.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 469, doi. 10.1007/s10689-014-9711-x

By:

Koeneman, Margot;
Kruse, Arnold-Jan;
Sep, Simone;
Gubbels, Cynthia;
Slangen, Brigitte;
Gorp, Toon;
Lopes, Alberto;
Gomez-Garcia, Encarna;
Kruitwagen, Roy

Publication type:

Article

Intronic splicing mutations in PTCH1 cause Gorlin syndrome.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 477, doi. 10.1007/s10689-014-9712-9

By:

Bholah, Zaynab;
Smith, Miriam;
Byers, Helen;
Miles, Emma;
Evans, D.;
Newman, William

Publication type:

Article

Fertility and apparent genetic anticipation in Lynch syndrome.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 369, doi. 10.1007/s10689-014-9714-7

By:

Stupart, Douglas;
Win, Aung;
Jenkins, Mark;
Winship, Ingrid;
Goldberg, Paul;
Ramesar, Rajkumar

Publication type:

Article

Two Chinese pedigrees for adenomatous polyposis coli: new mutations at codon 1309 and predisposition to phenotypic variations.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 361, doi. 10.1007/s10689-014-9713-8

By:

Liao, Dai-Xiang;
Li, Bing;
Du, Xue-Mei;
Yu, Jun-Hui;
Chang, Hong;
Wu, Zhi-Qiang;
Hao, Hao-Jie;
Wang, You-Xin;
Han, Wei-Dong;
Cheng, Shu-jun;
Luo, Cheng-Hua

Publication type:

Article

Influence of family history on psychosocial distress and perceived need for treatment in prostate cancer survivors.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 481, doi. 10.1007/s10689-014-9715-6

By:

Dinkel, Andreas;
Kornmayer, Marielouise;
Gschwend, Jürgen;
Marten-Mittag, Birgitt;
Herschbach, Peter;
Herkommer, Kathleen

Publication type:

Article

Attitudes and compliance of clinical management after genetic testing for hereditary breast and ovarian cancer among high-risk Southern Chinese females with breast cancer history.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 423, doi. 10.1007/s10689-014-9706-7

By:

Kwong, Ava;
Chu, Annie;
Wu, Christine;
Tse, Desiree

Publication type:

Article

Duplex value of caveolin-1 in non-small cell lung cancer: a meta analysis.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 449, doi. 10.1007/s10689-014-9707-6

By:

Chen, Dali;
Shen, Cheng;
Du, Heng;
Zhou, Yubin;
Che, Guowei

Publication type:

Article

Novel BRCA1 deleterious mutation (c.1918C>T) in familial breast and ovarian cancer syndrome who share a common ancestry.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 431, doi. 10.1007/s10689-014-9708-5

By:

Gabaldó Barrios, Xavier;
Sarabia Meseguer, María;
Alonso Romero, José;
Marín Vera, Miguel;
Marín Zafra, Gema;
Sánchez Henarejos, Pilar;
Sánchez Bermúdez, Ana;
Ruiz Espejo, Francisco

Publication type:

Article

Mosaic partial deletion of the PTEN gene in a patient with Cowden syndrome.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 459, doi. 10.1007/s10689-014-9709-4

By:

Salo-Mullen, Erin;
Shia, Jinru;
Brownell, Isaac;
Allen, Peter;
Girotra, Monica;
Robson, Mark;
Offit, Kenneth;
Guillem, Jose;
Markowitz, Arnold;
Stadler, Zsofia

Publication type:

Article

Analysis of patient reports on the referral process to two NSW cancer genetic services.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 333, doi. 10.1007/s10689-014-9710-y

By:

Butel-Simoes, Grace;
Spigelman, Allan

Publication type:

Article

Erratum to: Frequency of 5382insC mutation of BRCA1 gene among breast cancer patients: an experience from Eastern India.

Published in:

2014

By:

Chakraborty, Abhijit;
Mukhopadhyay, Ashis;
Bhattacharyya, Deboshree;
Bose, Chinmoy;
Choudhuri, Keya;
Mukhopadhyay, Soma;
Basak, Jayasri

Publication type:

Erratum

BRCA1 point mutations in premenopausal breast cancer patients from Central Sudan.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 437, doi. 10.1007/s10689-014-9717-4

By:

Biunno, Ida;
Aceto, Gitana;
Awadelkarim, Khalid;
Morgano, Annalisa;
Elhaj, Ahmed;
Eltayeb, Elgaylani;
Abuidris, Dafalla;
Elwali, Nasr;
Spinelli, Chiara;
Blasio, Pasquale;
Rovida, Ermanna;
Mariani-Costantini, Renato

Publication type:

Article

An unusual case of familial adenomatous polyposis with very early symptom occurrence.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 375, doi. 10.1007/s10689-014-9718-3

By:

Ponz de Leon, Maurizio;
Bianchini, Maria;
Reggiani-Bonetti, Luca;
Pedroni, Monica;
Gregorio, Carmela;
Merighi, Alberto;
Rossi, Giuseppina;
Magnani, Giulia;
Domati, Federica;
Cacciari, Alfredo

Publication type:

Article

A survey of the practice patterns of gynecologic oncologists dealing with hereditary cancer patients in Japan.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 489, doi. 10.1007/s10689-014-9719-2

By:

Tanabe, Noriko;
Shikama, Ayumi;
Bando, Hiroko;
Satoh, Toyomi;
Shimizu, Chikako

Publication type:

Article

BRCA1 founder mutations compared to ovarian cancer in Belarus.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 445, doi. 10.1007/s10689-014-9721-8

By:

Savanevich, Alena;
Oszurek, Oleg;
Lubiński, Jan;
Cybulski, Cezary;
Dębniak, Tadeusz;
Narod, Steven;
Gronwald, Jacek

Publication type:

Article

Limited diagnostic value of microsatellite instability associated pathology features in colorectal cancer.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 351, doi. 10.1007/s10689-014-9705-8

By:

Putten, Paul;
Lier, Margot;
Hage, Mariska;
Biermann, Katharina;
Rijssel, Reinier;
Westenend, Pieter;
Morreau, Hans;
Steyerberg, Ewout;
Dinjens, Winand;
Kuipers, Ernst;
Leerdam, Monique;
Krieken, J.

Publication type:

Article

Evaluating the utilization of educational materials in communicating about Lynch syndrome to at-risk relatives.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 381, doi. 10.1007/s10689-014-9720-9

By:

Dilzell, Kristen;
Kingham, Kerry;
Ormond, Kelly;
Ladabaum, Uri

Publication type:

Article

Genetics of endometrial cancer.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 499, doi. 10.1007/s10689-014-9722-7

By:

Shai, Ayelet;
Segev, Yakir;
Narod, Steven

Publication type:

Article

Nucleotide variants of the cancer predisposing gene CDH1 and the risk of non-syndromic cleft lip with or without cleft palate.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 415, doi. 10.1007/s10689-014-9727-2

By:

Hozyasz, Kamil;
Mostowska, Adrianna;
Wójcicki, Piotr;
Lasota, Agnieszka;
Offert, Barbara;
Balcerek, Adam;
Dunin-Wilczyńska, Izabella;
Jagodziński, Paweł

Publication type:

Article

How harmful is genetic testing for familial adenomatous polyposis (FAP) in young children; the parents' experience.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 391, doi. 10.1007/s10689-014-9724-5

By:

Kattentidt-Mouravieva, Anna;
Heijer, M.;
Kessel, I.;
Wagner, A.

Publication type:

Article

Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignancies.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 507, doi. 10.1007/s10689-014-9725-4

By:

Renella, R.;
Carnevale, J.;
Schneider, K.;
Hornick, J.;
Rana, H.;
Janeway, K.

Publication type:

Article

'Would you test your children without their consent?' and other sticky dilemmas in the field of cancer genetic testing.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 345, doi. 10.1007/s10689-014-9723-6

By:

Brierley, Karina;
Bonadies, Danielle;
Moyer, Anne;
Matloff, Ellen

Publication type:

Article

A founder MLH1 mutation in Lynch syndrome families from Piedmont, Italy, is associated with an increased risk of pancreatic tumours and diverse immunohistochemical patterns.

Published in:

Familial Cancer, 2014, v. 13, n. 3, p. 401, doi. 10.1007/s10689-014-9726-3

By:

Borelli, Iolanda;
Casalis Cavalchini, Guido;
Del Peschio, Serena;
Micheletti, Monica;
Venesio, Tiziana;
Sarotto, Ivana;
Allavena, Anna;
Delsedime, Luisa;
Barberis, Marco;
Mandrile, Giorgia;
Berchialla, Paola;
Ogliara, Paola;
Bracco, Cecilia;
Pasini, Barbara

Publication type:

Article