Works matching IS 13899600 AND DT 2020 AND VI 19 AND IP 1

Results: 10

Renal cell carcinoma in young FH mutation carriers: case series and review of the literature.
Published in:
Familial Cancer, 2020, v. 19, n. 1, p. 55, doi. 10.1007/s10689-019-00155-3
By:
- Hol, J. A.;
- Jongmans, M. C. J.;
- Littooij, A. S.;
- de Krijger, R. R.;
- Kuiper, R. P.;
- van Harssel, J. J. T.;
- Mensenkamp, A.;
- Simons, M.;
- Tytgat, G. A. M.;
- van den Heuvel-Eibrink, M. M.;
- van Grotel, M.
Publication type:
Article
'We don't know for sure': discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultations.
Published in:
Familial Cancer, 2020, v. 19, n. 1, p. 65, doi. 10.1007/s10689-019-00154-4
By:
- Medendorp, Niki M.;
- Hillen, Marij A.;
- van Maarschalkerweerd, Pomme E. A.;
- Aalfs, Cora M.;
- Ausems, Margreet G. E. M.;
- Verhoef, Senno;
- van der Kolk, Lizet E.;
- Berger, Lieke P. V.;
- Wevers, Marijke R.;
- Wagner, Anja;
- Caanen, Barbara A. H.;
- Stiggelbout, Anne M.;
- Smets, Ellen M. A.
Publication type:
Article
Radiotherapy-induced malignancies in breast cancer patients with TP53 pathogenic germline variants (Li–Fraumeni syndrome).
Published in:
Familial Cancer, 2020, v. 19, n. 1, p. 47, doi. 10.1007/s10689-019-00153-5
By:
- Petry, Vanessa;
- Bonadio, Renata Colombo;
- Cagnacci, Allyne Queiroz Carneiro;
- Senna, Luiz Antonio Leite;
- Campos, Roberta do Nascimento Galvão;
- Cotti, Guilherme Cutait;
- Hoff, Paulo M.;
- Fragoso, Maria Candida Barisson Villares;
- Estevez-Diz, Maria del Pilar
Publication type:
Article
MLH1 promoter hypermethylation: are you absolutely sure about the absence of MLH1 germline mutation? About a new case.
Published in:
Familial Cancer, 2020, v. 19, n. 1, p. 11, doi. 10.1007/s10689-019-00151-7
By:
- Kientz, Caroline;
- Prieur, Fabienne;
- Clemenson, Alix;
- Joly, Marie-Odile;
- Stachowicz, Marie-Laure;
- Auclair, Jessie;
- Attignon, Valéry;
- Schiappa, Renaud;
- Wang, Qing
Publication type:
Article
Abstracts of the 4th meeting of the European Hereditary Tumour Group, Barcelona, Spain, October 17–19th, 2019.
Published in:
2020
Publication type:
Calendar
Clear cell chondrosarcoma in Von Hippel-Lindau disease.
Published in:
Familial Cancer, 2020, v. 19, n. 1, p. 41, doi. 10.1007/s10689-019-00149-1
By:
- Dreijerink, Koen M. A.;
- van Leeuwaarde, Rachel S.;
- Hackeng, Wenzel M.;
- Giles, Rachel H.;
- de Leng, Wendy W. J.;
- Jutte, Paul C.;
- Suurmeijer, Albert J. H.;
- van Nesselrooij, Bernadette P. M.;
- Brosens, Lodewijk A. A.
Publication type:
Article
Neurofibromatosis type 2 discordance in monozygous twins.
Published in:
Familial Cancer, 2020, v. 19, n. 1, p. 37, doi. 10.1007/s10689-019-00148-2
By:
- Amico, S.;
- Smith, P.;
- Tobi, S.;
- Perry, M.;
- Wallace, A.;
- Evans, D. G.
Publication type:
Article
Long-term positive psychological outcomes in an Australian pancreatic cancer screening program.
Published in:
Familial Cancer, 2020, v. 19, n. 1, p. 23, doi. 10.1007/s10689-019-00147-3
By:
- O'Neill, R. S.;
- Meiser, B.;
- Emmanuel, S.;
- Williams, D. B.;
- Stoita, A.
Publication type:
Article
A unique case of two somatic APC mutations in an early onset cribriform-morular variant of papillary thyroid carcinoma and overview of the literature.
Published in:
Familial Cancer, 2020, v. 19, n. 1, p. 15, doi. 10.1007/s10689-019-00146-4
By:
- Aydemirli, M. D.;
- van der Tuin, K.;
- Hes, F. J.;
- van den Ouweland, A. M. W.;
- van Wezel, T.;
- Kapiteijn, E.;
- Morreau, H.
Publication type:
Article
Novel candidates in early-onset familial colorectal cancer.
Published in:
Familial Cancer, 2020, v. 19, n. 1, p. 1, doi. 10.1007/s10689-019-00145-5
By:
- Jansen, Anne M. L.;
- Ghosh, Pradipta;
- Dakal, Tikam C.;
- Slavin, Thomas P.;
- Boland, C. Richard;
- Goel, Ajay
Publication type:
Article