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Human Mutation|February 1, 2012
Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic featuresAllen N Lamb, Jill A Rosenfeld, Nicholas J Neill, et al.Genome Announcements|January 11, 2014
Draft Genome Sequence of Clostridium mangenotii TR, Isolated from the Fecal Material of a Timber RattlesnakeRichard W McLaughlin, Philip A Cochran, Scot E Dowd, et al.European Journal of Human Genetics : EJHG|April 9, 2015
PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndromeJulián Nevado, Jill A Rosenfeld, Rocío Mena, et al.Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|August 27, 2025
Multi-centre Investigation of Cardiac Diffusion Tensor Imaging in Healthy Volunteers by SCMR Cardiac Diffusion Special Interest Group NETwork (SIGNET)Irvin Teh, Kévin Moulin, Pedro F Ferreira, et al.The New England Journal of Medicine|April 16, 2025
Tecovirimat for Clade I MPXV Infection in the Democratic Republic of Congo, Rosine Ali, Jules Alonga, et al.Human Mutation|September 28, 2011
Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeatsPaweł Stankiewicz, Shashikant Kulkarni, Avinash V Dharmadhikari, et al.Autophagy|February 26, 2021
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1Daniel J Klionsky, Amal Kamal Abdel-Aziz, Sara Abdelfatah, et al.Pageof 88