Currall BB, Antolik CW, Collins RL, Talkowski ME. Next Generation Sequencing of Prenatal Structural Chromosomal Rearrangements Using Large-Insert Libraries. Methods Mol Biol. 2019;1885:251-265. doi:10.1007/978-1-4939-8889-1_17PubMedDOIGoogle Scholar

Currall BB, Chen M, Sallari RC, et al. Loss of LDAH associated with prostate cancer and hearing loss. Hum Mol Genet. 2018;27(24):4194-4203. doi:10.1093/hmg/ddy310PubMedDOIGoogle Scholar

Zepeda-Mendoza CJ, Ibn-Salem J, Kammin T, et al. Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal Rearrangements. Am J Hum Genet. 2017;101(2):206-217. doi:10.1016/j.ajhg.2017.06.011PubMedDOIGoogle Scholar

Luukkonen TM, Mehrjouy MM, Pöyhönen M, et al. Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes. Mol Genet Genomic Med. 2018;6(1):56-68. doi:10.1002/mgg3.346PubMedDOIGoogle Scholar

McPherson AW, Roth A, Ha G, et al. ReMixT: clone-specific genomic structure estimation in cancer. Genome Biol. 2017;18(1):140. doi:10.1186/s13059-017-1267-2PubMedDOIGoogle Scholar

Sun S, Yadav V, Billmyre B, et al. Fungal genome and mating system transitions facilitated by chromosomal translocations involving intercentromeric recombination. PLoS Biol. 2017;15(8):e2002527. doi:10.1371/journal.pbio.2002527PubMedDOIGoogle Scholar

Pikman Y, Stegmaier K. Targeted therapy for fusion-driven high-risk acute leukemia. Blood. 2018;132(12):1241-1247. doi:10.1182/blood-2018-04-784157PubMedDOIGoogle Scholar

Wilch ES, Morton CC. Historical and Clinical Perspectives on Chromosomal Translocations. Adv Exp Med Biol. 2018;1044:1-14. doi:10.1007/978-981-13-0593-1_1PubMedDOIGoogle Scholar

Christian S, Merz C, Evans L, et al. The novel dihydroorotate dehydrogenase (DHODH) inhibitor BAY 2402234 triggers differentiation and is effective in the treatment of myeloid malignancies. Leukemia. 2019;33(10):2403-2415. doi:10.1038/s41375-019-0461-5PubMedDOIGoogle Scholar

Dong Z, Wang H, Chen H, et al. Identification of balanced chromosomal rearrangements previously unknown among participants in the 1000 Genomes Project: implications for interpretation of structural variation in genomes and the future of clinical cytogenetics. Genet Med. 2018;20(7):697-707. doi:10.1038/gim.2017.170PubMedGoogle ScholarDOI