Showing results (1291-1300 of 2,771) with videos related to

Sort By:
Pageof 278
BMC Medical Genomics|March 6, 2024
Correlation between large rearrangements and patient phenotypes in NF1 deletion syndrome: an update and reviewLaurence Pacot, Milind Girish, Samantha Knight, et al.
BMC Medical Genomics|March 5, 2024
Heterozygous truncating variant of TAOK1 in a boy with periventricular nodular heterotopia: a case report and literature review of TAOK1-related neurodevelopmental disordersAnna Cavalli, Stefano Giuseppe Caraffi, Susanna Rizzi, et al.
BMC Medical Genomics|March 5, 2024
Development and proof-of-concept demonstration of a clinical metagenomics method for the rapid detection of bloodstream infectionLluis Moragues-Solanas, Thanh Le-Viet, Elinor McSorley, et al.
BMC Medical Genomics|February 26, 2024
Causal effects between circulating immune cells and heart failure: evidence from a bidirectional Mendelian randomization studyRutao Bian, Xuegong Xu, Zishuang Li
BMC Medical Genomics|February 23, 2024
Identifying functional subtypes of IgA nephropathy based on three machine learning algorithms and WGCNAHongbiao Ren, Wenhua Lv, Zhenwei Shang, et al.
BMC Medical Genomics|February 21, 2024
Prognosis and biological function of SGOL1 in clear cell renal cell carcinoma: a multiomics analysisZezhong Yang, Yunzhong Jiang, Lu Wang, et al.
BMC Medical Genomics|February 28, 2024
The influence of Nrf2 gene promoter methylation on gene expression and oxidative stress parameters in preeclampsiaSaba Zakeri, Zohreh Rahimi, Nayebali Rezvani, et al.
BMC Medical Genomics|February 21, 2024
Proteome-wide mendelian randomization investigates potential associations in heart failure and its etiology: emphasis on PCSK9Lichao Lin, Huizhen Yu, Yan Xue, et al.
BMC Medical Genomics|November 23, 2023
Retinal nerve fibre layer thinning and corneal nerve loss in patients with Bardet-Biedl syndromeAziz Belkadi, Gaurav Thareja, Adnan Khan, et al.
BMC Medical Genomics|November 17, 2023
Mutation spectrum, expression profiling, and prognosis evaluation of Fanconi anemia signaling pathway genes for 4259 patients with myelodysplastic syndromes or acute myeloid leukemiaLixian Chang, Li Zhang, Beibei Zhao, et al.
Pageof 278