Inherited heterozygous Fanconi anemia gene mutations in a therapy-related CMML patient with a rare NUP98-HOXC11 fusion: A case report

MLA

Kefeng Shen, et al. “Inherited Heterozygous Fanconi Anemia Gene Mutations in a Therapy-Related CMML Patient with a Rare NUP98-HOXC11 Fusion: A Case Report.” Frontiers in Oncology, vol. 12, Oct. 2022. EBSCOhost, https://doi.org/10.3389/fonc.2022.1036511.

APA

Kefeng Shen, Meilan Zhang, Jiachen Wang, Wei Mu, Jin Wang, Chunyan Wang, Shugang Xing, Zhenya Hong, & Min Xiao. (2022). Inherited heterozygous Fanconi anemia gene mutations in a therapy-related CMML patient with a rare NUP98-HOXC11 fusion: A case report. Frontiers in Oncology, 12. https://doi.org/10.3389/fonc.2022.1036511

Chicago

Kefeng Shen, Meilan Zhang, Jiachen Wang, Wei Mu, Jin Wang, Chunyan Wang, Shugang Xing, Zhenya Hong, and Min Xiao. 2022. “Inherited Heterozygous Fanconi Anemia Gene Mutations in a Therapy-Related CMML Patient with a Rare NUP98-HOXC11 Fusion: A Case Report.” Frontiers in Oncology 12 (October). doi:10.3389/fonc.2022.1036511.