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BMC Medical Genomics|March 29, 2022
Analysis of the genotype-phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patientsYing Fu, Shasha Huang, Xue Gao, et al.BMC Medical Genomics|March 31, 2022
Evaluation of genetic variants using chromosomal microarray analysis for fetuses with polyhydramniosXiaoqing Wu, Ying Li, Na Lin, et al.BMC Medical Genomics|August 31, 2018
Differentially expressed proteins in positive versus negative HNSCC lymph nodesAlessandra Vidotto, Giovana M Polachini, Marina de Paula-Silva, et al.BMC Medical Genomics|March 8, 2022
Genetic diagnosis of pseudomyxoma peritonei originating from mucinous borderline tumor inside an ovarian teratomaAyumi Taguchi, Hirofumi Rokutan, Katsutoshi Oda, et al.BMC Medical Genomics|March 4, 2022
Network analysis of atherosclerotic genes elucidates druggable targetsSheuli Kangsa Banik, Somorita Baishya, Anupam Das Talukdar, et al.BMC Medical Genomics|June 15, 2018
Calculating the statistical significance of rare variants causal for Mendelian and complex disordersAliz R Rao, Stanley F NelsonBMC Medical Genomics|April 30, 2010
Signaling pathway networks mined from human pituitary adenoma proteomics dataXianquan Zhan, Dominic M DesiderioBMC Medical Genomics|May 8, 2009
High-resolution analysis of copy number alterations and associated expression changes in ovarian tumorsPeter M Haverty, Lawrence S Hon, Joshua S Kaminker, et al.BMC Medical Genomics|March 11, 2009
Distinct gene subsets in pterygia formation and recurrence: dissecting complex biological phenomenon using genome wide expression dataLouis Tong, Jaime Chew, Henry Yang, et al.BMC Medical Genomics|December 26, 2008
Global gene expression analyses of bystander and alpha particle irradiated normal human lung fibroblasts: synchronous and differential responsesShanaz A Ghandhi, Benjamin Yaghoubian, Sally A AmundsonPageof 276