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Clinical Genetics|October 17, 2013
Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotypeI Filges, E Nosova, E Bruder, et al.Angewandte Chemie (International Ed. in English)|October 21, 2015
Sulfur-Limonene Polysulfide: A Material Synthesized Entirely from Industrial By-Products and Its Use in Removing Toxic Metals from Water and SoilMichael P Crockett, Austin M Evans, Max J H Worthington, et al.Angewandte Chemie (International Ed. in English)|January 19, 2018
Electrocatalytic Activity of a 2D Phosphorene-Based Heteroelectrocatalyst for Photoelectrochemical CellsMunkhbayar Batmunkh, Aabhash Shrestha, Munkhjargal Bat-Erdene, et al.Human Mutation|December 16, 2015
Mutations in FLNC are Associated with Familial Restrictive CardiomyopathyAndreas Brodehl, Raechel A Ferrier, Sara J Hamilton, et al.Journal of the National Cancer Institute|July 24, 2013
Cancer incidence trends among native Hawaiians and other Pacific Islanders in the United States, 1990-2008Lihua Liu, Anne-Michelle Noone, Scarlett Lin Gomez, et al.Pediatric Rheumatology Online Journal|October 30, 2019
Complexity in unclassified auto-inflammatory disease: a case report illustrating the potential for disease arising from the allelic burden of multiple variantsLori B Tucker, Lovro Lamot, Iwona Niemietz, et al.Journal of the National Cancer Institute|July 24, 2013
Cancer incidence trends among Asian American populations in the United States, 1990-2008Scarlett Lin Gomez, Anne-Michelle Noone, Daphne Y Lichtensztajn, et al.Journal of Human Genetics|January 24, 2019
A distinct neurodevelopmental syndrome with intellectual disability, autism spectrum disorder, characteristic facies, and macrocephaly is caused by defects in CHD8Heba Yasin, William T Gibson, Sylvie Langlois, et al.The Journal of Chemical Physics|February 4, 2012
Experimental verification of strong rotational dependence of fluorescence and predissociation yield in the b1Πu(v = 1) level of 14N2C Y Robert Wu, D L Judge, M-H Tsai, et al.Nature Genetics|October 5, 2001
The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxinM C Moreira, C Barbot, N Tachi, et al.Pageof 68