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Human Genomics|June 28, 2018
Caution needs to be taken when assigning transcription start sites to ends of protein-coding genes: a rebuttalNiv Sabath, Anna Vilborg, Joan A Steitz, et al.Human Genomics|April 25, 2023
Identification of four novel large deletions and complex variants in the α-globin locus in Chinese populationXiuqin Bao, Jicheng Wang, Danqing Qin, et al.Human Genomics|April 25, 2023
The spectrum of phenylalanine hydroxylase variants and genotype-phenotype correlation in phenylketonuria patients in Gansu, ChinaChuan Zhang, Pei Zhang, Yousheng Yan, et al.Human Genomics|May 13, 2023
Autosomal recessive congenital cataract is associated with a novel 4-bp splicing deletion mutation in a novel C10orf71 human geneM Chograni, H M Alahdal, M RejiliHuman Genomics|March 28, 2023
Community data-driven approach to identify pathogenic founder variants for pan-ethnic carrier screening panelsYaron Einhorn, Moshe Einhorn, Alina Kurolap, et al.Human Genomics|November 27, 2012
Association of genome variations in the renin-angiotensin system with physical performanceArgyro Sgourou, Vassilis Fotopoulos, Vassilis Kontos, et al.Human Genomics|December 14, 2011
Neurofibromatosis type 1-associated tumours: their somatic mutational spectrum and pathogenesisSebastian Laycock-van Spyk, Nick Thomas, David N Cooper, et al.Human Genomics|December 14, 2011
Overview of biological database mapping services for interoperation between different 'omics' datasetsShweta S Chavan, John D Shaughnessy, Ricky D EdmondsonHuman Genomics|December 12, 2019
The multi-faceted functioning portrait of LRF/ZBTB7ACaterina Constantinou, Magda Spella, Vasiliki Chondrou, et al.Human Genomics|January 26, 2019
The association of functional polymorphisms in genes expressed in endothelial cells and smooth muscle cells with the myocardial infarctionYilan Li, Shipeng Wang, Dandan Zhang, et al.Pageof 112