Works matching IS 10452257 AND DT 2022 AND VI 61 AND IP 6

Results: 8

Principles of molecular testing for hereditary cancer.
Published in:
Genes, Chromosomes & Cancer, 2022, v. 61, n. 6, p. 356, doi. 10.1002/gcc.23048
By:
- Mighton, Chloe;
- Lerner‐Ellis, Jordan P.
Publication type:
Article
Methylation classifiers: Brain tumors, sarcomas, and what's next.
Published in:
Genes, Chromosomes & Cancer, 2022, v. 61, n. 6, p. 346, doi. 10.1002/gcc.23041
By:
- Koelsche, Christian;
- von Deimling, Andreas
Publication type:
Article
Wholistic approach: Transcriptomic analysis and beyond using archival material for molecular diagnosis.
Published in:
Genes, Chromosomes & Cancer, 2022, v. 61, n. 6, p. 382, doi. 10.1002/gcc.23026
By:
- Macagno, Nicolas;
- Pissaloux, Daniel;
- de la Fouchardière, Arnaud;
- Karanian, Marie;
- Lantuejoul, Sylvie;
- Galateau Salle, Françoise;
- Meurgey, Alexandra;
- Chassagne‐Clement, Catherine;
- Treilleux, Isabelle;
- Renard, Caroline;
- Roussel, Juliette;
- Gervasoni, Julie;
- Cockenpot, Vincent;
- Crozes, Carole;
- Baltres, Aline;
- Houlier, Aurélie;
- Paindavoine, Sandrine;
- Alberti, Laurent;
- Duc, Adeline;
- Le Loarer, Francois
Publication type:
Article
Advances in sarcoma molecular diagnostics.
Published in:
Genes, Chromosomes & Cancer, 2022, v. 61, n. 6, p. 332, doi. 10.1002/gcc.23025
By:
- Wang, Xue Qi;
- Goytain, Angela;
- Dickson, Brendan C.;
- Nielsen, Torsten Owen
Publication type:
Article
Computational methods and translational applications for targeted next‐generation sequencing platforms.
Published in:
Genes, Chromosomes & Cancer, 2022, v. 61, n. 6, p. 322, doi. 10.1002/gcc.23023
By:
- Luthra, Anisha;
- Mastrogiacomo, Brooke;
- Smith, Shaleigh A.;
- Chakravarty, Debyani;
- Schultz, Nikolaus;
- Sanchez‐Vega, Francisco
Publication type:
Article
Mismatch repair deficiency: The what, how and why it is important.
Published in:
Genes, Chromosomes & Cancer, 2022, v. 61, n. 6, p. 314, doi. 10.1002/gcc.23015
By:
- Olave, Maria C.;
- Graham, Rondell P.
Publication type:
Article
Assigning evidence to actionability: An introduction to variant interpretation in precision cancer medicine.
Published in:
Genes, Chromosomes & Cancer, 2022, v. 61, n. 6, p. 303, doi. 10.1002/gcc.22987
By:
- Horak, Peter;
- Leichsenring, Jonas;
- Goldschmid, Hannah;
- Kreutzfeldt, Simon;
- Kazdal, Daniel;
- Teleanu, Veronica;
- Endris, Volker;
- Gieldon, Laura;
- Allgäuer, Michael;
- Volckmar, Anna‐Lena;
- Dikow, Nicola;
- Renner, Marcus;
- Kirchner, Martina;
- Penzel, Roland;
- Ploeger, Carolin;
- Brandt, Regine;
- Seker‐Cin, Huriye;
- Budczies, Jan;
- Heilig, Christoph E.;
- Neumann, Olaf
Publication type:
Article
Issue Information.
Published in:
Genes, Chromosomes & Cancer, 2022, v. 61, n. 6, p. 299, doi. 10.1002/gcc.22963
Publication type:
Article