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Cancer Genetics|December 2, 2021
Investigation of discordant sibling pairs from hereditary breast cancer families and analysis of a rare PMS1 variantK K Landry, D J Seward, J A Dragon, et al.Cancer Genetics|November 19, 2013
Identification of predictive biomarkers for early diagnosis of larynx carcinoma based on microRNA expression dataYan Wang, Mingtao Chen, Zezhang Tao, et al.Cancer Genetics|July 15, 2014
Identifying molecular markers for the sensitive detection of residual atypical teratoid rhabdoid tumor cellsTu-Lan Vu-Han, Michael C Frühwald, Martin Hasselblatt, et al.Cancer Genetics|March 13, 2016
Clinical characteristics and genetic subtypes of Fanconi anemia in Saudi patientsYahya Ghazwani, Mohammed AlBalwi, Ibrahim Al-Abdulkareem, et al.Cancer Genetics|June 9, 2016
Lineage switch with t(6;11)(q27;q23) from T-cell lymphoblastic lymphoma to acute monoblastic leukemia at relapseYusuke Higuchi, Kenji Tokunaga, Yuko Watanabe, et al.Cancer Genetics|July 4, 2016
Evaluation of rs62527607 [GT] single nucleotide polymorphism located in BAALC gene in children with acute leukemia using mismatch PCR-RFLPMotahareh Nadimi, Soheila Rahgozar, Alireza Moafi, et al.Cancer Genetics|October 4, 2015
LAMTOR1-PRKCD and NUMA1-SFMBT1 fusion genes identified by RNA sequencing in aneurysmal benign fibrous histiocytoma with t(3;11)(p21;q13)Ioannis Panagopoulos, Ludmila Gorunova, Bodil Bjerkehagen, et al.Cancer Genetics|March 21, 2012
Characterization of the colorectal cancer-associated enhancer MYC-335 at 8q24: the role of rs67491583Sari Tuupanen, Jian Yan, Mikko Turunen, et al.Cancer Genetics|March 21, 2012
A t(17;22)(q21;q12) with partial ETV4 deletion in a soft tissue Ewing sarcomaAnne-Laure Rougemont, Dorothée Bouron-Dal Soglio, Natacha Patey-Mariaud de Serre, et al.Cancer Genetics|May 18, 2016
Establishing a murine xenograft-model for long-term analysis of factors inducing chromosomal instability in myelodysplastic syndrome: Pitfalls and successesAzam Salari, Kathrin Thomay, Kirsten Himmler, et al.Pageof 113