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Human Molecular Genetics|March 21, 1998
A novel gene that encodes a protein with a putative src homology 3 domain is a candidate gene for familial juvenile nephronophthisisS Saunier, J Calado, R Heilig, et al.Genome Research|June 14, 2003
An active non-LTR retrotransposon with tandem structure in the compact genome of the pufferfish Tetraodon nigroviridisLaurence Bouneau, Cécile Fischer, Catherine Ozouf-Costaz, et al.The Journal of Clinical Endocrinology and Metabolism|November 5, 1997
Genetic exclusion of 14 candidate genes in lipoatropic diabetes using linkage analysis in 10 consanguineous familiesC Vigouroux, E Khallouf, C Bourut, et al.Nature Genetics|November 1, 1994
A second locus for Marfan syndrome maps to chromosome 3p24.2-p25G Collod, M C Babron, G Jondeau, et al.Nature Genetics|March 1, 1994
A gene for achondroplasia-hypochondroplasia maps to chromosome 4pM Le Merrer, F Rousseau, L Legeai-Mallet, et al.Genomics|May 1, 1994
Genetic heterogeneity of Usher syndrome type 1 in French familiesD Larget-Piet, S Gerber, D Bonneau, et al.American Journal of Human Genetics|January 1, 1994
Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellitesA M Bowcock, J Tomfohrde, J Weissenbach, et al.Human Genetics|November 1, 1994
Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)E Plassart, A Elbaz, J V Santos, et al.Nature Genetics|March 1, 1994
Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European familiesB Fontaine, J Vale-Santos, K Jurkat-Rott, et al.Genome Research|March 1, 1996
Positional candidate genes for congenital chloride diarrhea suggested by high-resolution physical mapping in chromosome region 7q31P Höglund, S Haila, S W Scherer, et al.Pageof 46