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Gene|February 17, 2001
Architecture and anatomy of the genomic locus encoding the human leukemia-associated transcription factor RUNX1/AML1D Levanon, G Glusman, T Bangsow, et al.Clinical Genetics|July 4, 2015
SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosumG Heimer, D Marek-Yagel, E Eyal, et al.Nature Genetics|August 31, 2001
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathyI Eisenberg, N Avidan, T Potikha, et al.Pharmacogenetics|August 1, 1997
The UDP glycosyltransferase gene superfamily: recommended nomenclature update based on evolutionary divergenceP I Mackenzie, I S Owens, B Burchell, et al.Nature|March 10, 2001
Initial sequencing and analysis of the human genomeE S Lander, L M Linton, B Birren, et al.Pageof 9