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Human Genomics|June 10, 2016
Genetic risk factors for restenosis after percutaneous coronary intervention in Kazakh populationElena V Zholdybayeva, Yerkebulan A Talzhanov, Akbota M Aitkulova, et al.Human Genomics|September 18, 2015
MATWIN: bridging the gap between academic research and industryJosy Reiffers, Lucia RobertHuman Genomics|December 16, 2015
Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patientsEileen C P Lim, Maggie Brett, Angeline H M Lai, et al.Human Genomics|December 17, 2017
Early-life adversity and long-term neurobehavioral outcomes: epigenome as a bridge?Alexander M Vaiserman, Alexander K KoliadaHuman Genomics|February 21, 2018
Insights about genome function from spatial organization of the genomeShuvra Shekhar Roy, Ananda Kishore Mukherjee, Shantanu ChowdhuryHuman Genomics|February 19, 2018
APPLaUD: access for patients and participants to individual level uninterpreted genomic dataAdrian Thorogood, Jason Bobe, Barbara Prainsack, et al.Human Genomics|January 27, 2018
Identification of compound heterozygous variants in the noncoding RNU4ATAC gene in a Chinese family with two successive foetuses with severe microcephalyYe Wang, Xueli Wu, Liu Du, et al.Human Genomics|January 21, 2018
Identify Down syndrome transcriptome associations using integrative analysis of microarray database and correlation-interaction networkMin Chen, Jiayan Wang, Yingjun Luo, et al.Human Genomics|March 29, 2018
Large-scale discovery of previously undetected microRNAs specific to human liverBrenda C Minatel, Victor D Martinez, Kevin W Ng, et al.Human Genomics|May 1, 2009
Association of ADH1B and ALDH2 gene polymorphisms with alcohol dependence: a pilot study from IndiaMeera Vaswani, Pushplata Prasad, Suman KapurPageof 112