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International Journal of Immunopharmacology|May 1, 1994
Treatment of radiation disease by Nocardia fraction: possible effect of inflammatory cytokinesL Mandel, I Trebichavský, H Tlaskalová, et al.Nature|July 9, 1987
Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosomeR Heilig, C Lemaire, J L Mandel, et al.American Journal of Medical Genetics|April 1, 1992
Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in developmentD Devys, V Biancalana, F Rousseau, et al.American Journal of Medical Genetics|July 15, 1994
Non-specific X-linked mental retardation: linkage analysis in MRX2 and MRX4 families revisitedL J Hu, S Blumenfeld-Heyberger, A Hanauer, et al.European Journal of Human Genetics : EJHG|January 1, 1993
Striking founder effect for the fragile X syndrome in FinlandC Oudet, H von Koskull, A M Nordström, et al.Proceedings of the National Academy of Sciences of the United States of America|January 1, 1993
Gene in the region of the Friedreich ataxia locus encodes a putative transmembrane protein expressed in the nervous systemF Duclos, U Boschert, G Sirugo, et al.Human Molecular Genetics|July 1, 1992
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophyV Biancalana, F Serville, J Pommier, et al.Nucleic Acids Research|June 11, 1983
Isolation and characterization of cDNA clones for human skeletal muscle alpha actinA Hanauer, M Levin, R Heilig, et al.Genomics|July 15, 1994
A new human gene (DXS1357E) with ubiquitous expression, located in Xq28 adjacent to the adrenoleukodystrophy geneJ Mosser, C O Sarde, S Vicaire, et al.American Journal of Human Genetics|April 1, 1990
Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosomeR Feil, G Palmieri, M d'Urso, et al.Pageof 31