Showing results (441-450 of 467) with videos related to
Sort By:
Pageof 47
Nature|December 20, 2013
The complete genome sequence of a Neanderthal from the Altai MountainsKay Prüfer, Fernando Racimo, Nick Patterson, et al.American Journal of Human Genetics|July 14, 2015
The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and OpportunitiesJessica X Chong, Kati J Buckingham, Shalini N Jhangiani, et al.American Journal of Human Genetics|September 24, 2013
Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein armsMichael R Knowles, Lawrence E Ostrowski, Niki T Loges, et al.Nature Genetics|September 15, 2014
Refining analyses of copy number variation identifies specific genes associated with developmental delayBradley P Coe, Kali Witherspoon, Jill A Rosenfeld, et al.Nature Genetics|June 26, 2012
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromesJean-Baptiste Rivière, Ghayda M Mirzaa, Brian J O'Roak, et al.Science Translational Medicine|May 4, 2021
Viral genomes reveal patterns of the SARS-CoV-2 outbreak in Washington StateNicola F Müller, Cassia Wagner, Chris D Frazar, et al.Medrxiv : the Preprint Server for Health Sciences|June 9, 2020
A Genomic Survey of SARS-CoV-2 Reveals Multiple Introductions into Northern California without a Predominant LineageXianding Deng, Wei Gu, Scot Federman, et al.JAMA Neurology|May 10, 2016
Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary MosaicismGhayda M Mirzaa, Catarina D Campbell, Nadia Solovieff, et al.Science (New York, N.Y.)|June 9, 2018
High-resolution comparative analysis of great ape genomesZev N Kronenberg, Ian T Fiddes, David Gordon, et al.Nature|November 4, 2014
The contribution of de novo coding mutations to autism spectrum disorderIvan Iossifov, Brian J O'Roak, Stephan J Sanders, et al.Pageof 47