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Neurology|October 14, 2016
Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsyMark A Corbett, Susannah T Bellows, Melody Li, et al.
Neurology|August 21, 2015
SCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizuresKatherine B Howell, Jacinta M McMahon, Gemma L Carvill, et al.
Plastic and Reconstructive Surgery|September 16, 2022
Short-Term Administration of HIV Protease Inhibitor Saquinavir Improves Skull Bone Healing with Enhanced OsteoclastogenesisHaixia Liu, Yun Shen, Bingkun Zhao, et al.
Genome Research|October 22, 2015
Promoter-distal RNA polymerase II binding discriminates active from inactive CCAAT/ enhancer-binding protein beta binding sitesDaniel Savic, Brian S Roberts, Julia B Carleton, et al.
Genome Research|January 14, 2010
Evolutionary constraint facilitates interpretation of genetic variation in resequenced human genomesDavid L Goode, Gregory M Cooper, Jeremy Schmutz, et al.
Genome Research|April 21, 2021
Genome-wide strand asymmetry in massively parallel reporter activity favors genic strandsBrian S Roberts, E Christopher Partridge, Bryan A Moyers, et al.
Anatomical Record (Hoboken, N.J. : 2007)|November 10, 2009
Age-related changes in craniofacial morphology in GDF-8 (myostatin)-deficient miceLisa Vecchione, Jeffrey Miller, Craig Byron, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2010
Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesityRuxandra Bachmann-Gagescu, Heather C Mefford, Charles Cowan, et al.
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