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Nature|March 14, 1996
A comprehensive genetic map of the human genome based on 5,264 microsatellitesC Dib, S Fauré, C Fizames, et al.Genomics|March 20, 1995
High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1)I Wang, B Franco, G B Ferrero, et al.Nature|September 3, 2004
Hox cluster disintegration with persistent anteroposterior order of expression in Oikopleura dioicaHee-Chan Seo, Rolf Brudvik Edvardsen, Anne Dorthea Maeland, et al.Journal of Medical Genetics|February 1, 1997
Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophyI S Naom, M D'Alessandro, H Topaloglu, et al.Metabolomics : Official Journal of the Metabolomic Society|November 7, 2014
Novel metabolic features in <i>Acinetobacter baylyi</i> ADP1 revealed by a multiomics approachLucille Stuani, Christophe Lechaplais, Aaro V Salminen, et al.Human Molecular Genetics|August 14, 2003
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2Caroline Lefévre, Stéphanie Audebert, Florence Jobard, et al.Neurology|May 23, 2007
A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21G Stevanin, C Paternotte, P Coutinho, et al.American Journal of Human Genetics|December 1, 1996
The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locusG David, P Giunti, N Abbas, et al.Genome Research|March 3, 2004
Whole genome sequence comparisons and "full-length" cDNA sequences: a combined approach to evaluate and improve Arabidopsis genome annotationVanina Castelli, Jean-Marc Aury, Olivier Jaillon, et al.Human Molecular Genetics|April 4, 2001
Mutations in the gene encoding SLURP-1 in Mal de MeledaJ Fischer, B Bouadjar, R Heilig, et al.Pageof 46