Showing results (451-460 of 871) with videos related to
Sort By:
Pageof 88
The Journal of Pediatrics|January 31, 2016
Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1LGrace Yoon, Zeenat Malam, Tara Paton, et al.BMC Medical Genetics|March 29, 2011
Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential geneMohammad M Ghahramani Seno, Benjamin Y M Kwan, Ka Ki M Lee-Ng, et al.Journal of Physics. Condensed Matter : an Institute of Physics Journal|August 10, 2011
Evolution of quantum criticality in CeNi(9-x)Cu(x)Ge(4)L Peyker, C Gold, E-W Scheidt, et al.The Journal of Biological Chemistry|August 15, 1993
Structure and chromosomal localization of the human constitutive endothelial nitric oxide synthase geneP A Marsden, H H Heng, S W Scherer, et al.Gene|September 5, 1998
Genomic structure of the human congenital chloride diarrhea (CLD) geneS Haila, P Höglund, S W Scherer, et al.Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|January 9, 2018
Copy Number Variation Analysis of 100 Twin Pairs Enriched for Neurodevelopmental DisordersSofia Stamouli, Britt-Marie Anderlid, Charlotte Willfors, et al.Genes|August 6, 2021
Contribution of Multiple Inherited Variants to Autism Spectrum Disorder (ASD) in a Family with 3 Affected SiblingsJasleen Dhaliwal, Ying Qiao, Kristina Calli, et al.The Journal of Biological Chemistry|July 6, 2004
Post-transcriptional regulation of endothelial nitric-oxide synthase by an overlapping antisense mRNA transcriptG Brett Robb, Andrew R Carson, Sharon C Tai, et al.Genes|February 25, 2022
Mutational Landscape of Autism Spectrum Disorder Brain TissueMarc Woodbury-Smith, Sylvia Lamoureux, Ghausia Begum, et al.Systematic Reviews|January 11, 2013
Protocol for a systematic review on the extent of non-publication of research studies and associated study characteristicsSusan Portalupi, Erik von Elm, Christine Schmucker, et al.Pageof 88