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

Results: 10

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

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

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

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

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