Terms: = Germ cell tumor AND USP6, TRE2, 9098, ENSG00000129204, TRE17, Tre-2, HRP1 AND Diagnosis
3 results:
1. Whole Exome Sequencing of Multiple Atypical Meningiomas in a Patient without History of Neurofibromatosis Type II: A Case Report.
Lyu J; Quan Y; Wang JB; Gong SP
Am J Case Rep; 2020 May; 21():e923928. PubMed ID: 32461543
[TBL] [Abstract] [Full Text] [Related]
2. An update of molecular pathology of bone tumors. Lessons learned from investigating samples by next generation sequencing.
Baumhoer D; Amary F; Flanagan AM
Genes Chromosomes Cancer; 2019 Feb; 58(2):88-99. PubMed ID: 30582658
[TBL] [Abstract] [Full Text] [Related]
3. Copy number alterations determined by single nucleotide polymorphism array testing in the clinical laboratory are indicative of gene fusions in pediatric cancer patients.
Busse TM; Roth JJ; Wilmoth D; Wainwright L; Tooke L; Biegel JA
Genes Chromosomes Cancer; 2017 Oct; 56(10):730-749. PubMed ID: 28597942
[TBL] [Abstract] [Full Text] [Related]
