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BMC Biology|August 1, 2017
The house spider genome reveals an ancient whole-genome duplication during arachnid evolutionEvelyn E Schwager, Prashant P Sharma, Thomas Clarke, et al.
American Journal of Human Genetics|August 27, 2021
COPB2 loss of function causes a coatopathy with osteoporosis and developmental delayRonit Marom, Lindsay C Burrage, Rossella Venditti, et al.
Human Mutation|March 28, 2022
Phenotypic and mutational spectrum of ROR2-related Robinow syndromeAriadne R Lima, Barbara M Ferreira, Chaofan Zhang, et al.
Nature|April 13, 2012
Patterns and rates of exonic de novo mutations in autism spectrum disordersBenjamin M Neale, Yan Kou, Li Liu, et al.
Environmental Science & Technology|April 11, 2018
The Toxicogenome of Hyalella azteca: A Model for Sediment Ecotoxicology and Evolutionary ToxicologyHelen C Poynton, Simone Hasenbein, Joshua B Benoit, et al.
American Journal of Human Genetics|August 4, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human HematopoiesisLinda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
BMC Genomics|November 23, 2018
The genome of the water strider Gerris buenoi reveals expansions of gene repertoires associated with adaptations to life on the waterDavid Armisén, Rajendhran Rajakumar, Markus Friedrich, et al.
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