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BMC Bioinformatics|November 9, 2006
Automated recognition of malignancy mentions in biomedical literatureYang Jin, Ryan T McDonald, Kevin Lerman, et al.BMC Bioinformatics|February 6, 2010
CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnosticsXiaowu Gai, Juan C Perin, Kevin Murphy, et al.Chemical Science|August 30, 2018
Reactivity studies on [Cp'Fe(μ-I)]<sub>2</sub>: nitrido-, sulfido- and diselenide iron complexes derived from pseudohalide activationMatthias Reiners, Miyuki Maekawa, Constantin G Daniliuc, et al.BMC Bioinformatics|July 23, 2014
Clinical phenotype-based gene prioritization: an initial study using semantic similarity and the human phenotype ontologyAaron J Masino, Elizabeth T Dechene, Matthew C Dulik, et al.Oncogene|April 15, 2005
Definition and characterization of a region of 1p36.3 consistently deleted in neuroblastomaPeter S White, Patricia M Thompson, Takahiro Gotoh, et al.Inorganic Chemistry|January 6, 2004
Synthesis of Pt(dpk)Cl(4) and the reversible hydration to Pt(dpk-O-OH)Cl(3).H-phenCl: X-ray, spectroscopic, and electrochemical characterizationKatherine N Crowder, Stephanie J Garcia, Rebekah L Burr, et al.Cancer Research|November 20, 2002
Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13John M Maris, Matthew J Weiss, Yael Mosse, et al.Journal of the National Cancer Institute|June 26, 2008
CHD5, a tumor suppressor gene deleted from 1p36.31 in neuroblastomasTomoyuki Fujita, Jun Igarashi, Erin R Okawa, et al.Investigative Ophthalmology & Visual Science|October 27, 2007
Mutations in the UBIAD1 gene on chromosome short arm 1, region 36, cause Schnyder crystalline corneal dystrophyJayne S Weiss, Howard S Kruth, Helena Kuivaniemi, et al.Plos One|May 3, 2013
Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disordersMaria Tropeano, Joo Wook Ahn, Richard J B Dobson, et al.Pageof 12