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BMC Medical Genomics|April 4, 2020
Somatic synonymous mutations in regulatory elements contribute to the genetic aetiology of melanomaDi Zhang, Junfeng Xia
BMC Medical Genomics|April 4, 2020
Prediction of circRNA-disease associations based on inductive matrix completionMenglu Li, Mengya Liu, Yannan Bin, et al.
BMC Medical Genomics|July 31, 2021
Novel method of real-time PCR-based screening for common fetal trisomiesSo Yeon Kim, Seung Mi Lee, Sun Min Kim, et al.
BMC Medical Genomics|July 31, 2021
Variation p.R1045H in MYH7 correlated with hypertrophic cardiomyopathy in a Chinese pedigreeYan Zhang, Yiyi Shang, Luo Liu, et al.
BMC Medical Genomics|July 28, 2021
HELLS serves as a poor prognostic biomarker and its downregulation reserves the malignant phenotype in pancreatic cancerFeng-Jiao Wang, Yan-Hua Jing, Chien-Shan Cheng, et al.
BMC Medical Genomics|July 29, 2021
Characterization of DNA lesions associated with cell-free DNA by targeted deep sequencingSeung-Ho Shin, Woong-Yang Park, Donghyun Park
BMC Medical Genomics|July 15, 2021
Somatic mutations in benign breast disease tissues and association with breast cancer riskStacey J Winham, Chen Wang, Ethan P Heinzen, et al.
BMC Medical Genomics|July 5, 2022
Association of SNPs in the FK-506 binding protein (FKBP5) gene among Han Chinese women with polycystic ovary syndromeXinyue Ma, Zhao Wang, Changming Zhang, et al.
BMC Medical Genomics|May 5, 2022
Copy number variation of urine exfoliated cells by low-coverage whole genome sequencing for diagnosis of prostate adenocarcinoma: a prospective cohort studyYouyan Guan, Xiaobing Wang, Kaopeng Guan, et al.
BMC Medical Genomics|June 19, 2022
Novel copy number variations within SYCE1 caused meiotic arrest and non-obstructive azoospermiaYuhua Huang, Ruhui Tian, Junwei Xu, et al.
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