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Human Genomics|July 14, 2021
Coding and noncoding variants in EBF3 are involved in HADDS and simplex autismEvin M Padhi, Tristan J Hayeck, Zhang Cheng, et al.Human Genomics|October 3, 2020
Practicing precision medicine with intelligently integrative clinical and multi-omics data analysisZeeshan AhmedHuman Genomics|December 31, 2022
Digital PCR-based evaluation of nucleic acid extraction kit performance for the co-purification of cell-free DNA and RNAJill Deleu, Kathleen Schoofs, Anneleen Decock, et al.Human Genomics|December 19, 2022
Identification of a minimum number of genes to predict triple-negative breast cancer subgroups from gene expression profilesLaila Akhouayri, Paola Ostano, Maurizia Mello-Grand, et al.Human Genomics|December 19, 2022
Preimplantation genetic testing for aneuploidy: challenges in clinical practiceHui Yang, Andrew Thomas DeWan, Mayur M Desai, et al.Human Genomics|December 2, 2022
Pan-cancer illumination of TRIM gene family reveals immunology regulation and potential therapeutic implicationsYueying Gao, Tao Pan, Gang Xu, et al.Human Genomics|July 25, 2022
RNA modification-related variants in genomic loci associated with body mass indexJingyun Wu, Mimi Wang, Limin Han, et al.Human Genomics|July 19, 2022
Genetic etiology and clinical challenges of phenylketonuriaNasser A Elhawary, Imad A AlJahdali, Iman S Abumansour, et al.Human Genomics|April 21, 2022
Impaired phosphate transport in SLC34A2 variants in patients with pulmonary alveolar microlithiasisÅsa Lina M Jönsson, Nati Hernando, Thomas Knöpfel, et al.Human Genomics|July 24, 2010
Characterisation of a functional intronic polymorphism in the human growth hormone (GH1) geneDavid S Millar, Martin Horan, Nadia A Chuzhanova, et al.Pageof 112