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Human Molecular Genetics|February 1, 1994
Isolation of yeast artificial chromosome clones from 54 polymorphic loci mapped with high odds on human chromosome 4J B Fan, J DeYoung, R Lagacé, et al.European Journal of Human Genetics : EJHG|January 1, 1997
Nephropathic cystinosis (CTNS-LSB): construction of a YAC contig comprising the refined critical region on chromosome 17p13U Peters, G Senger, M Rählmann, et al.Science (New York, N.Y.)|November 29, 2005
Vertebrate-type intron-rich genes in the marine annelid Platynereis dumeriliiFlorian Raible, Kristin Tessmar-Raible, Kazutoyo Osoegawa, et al.Nature|December 8, 1994
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related geneJ W Foster, M A Dominguez-Steglich, S Guioli, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|November 29, 1995
The role of SOX9 in autosomal sex reversal and campomelic dysplasiaA J Schafer, M A Dominguez-Steglich, S Guioli, et al.The Journal of Clinical Endocrinology and Metabolism|November 1, 1994
Fine structure mapping of the human X-linked hypophosphatemic rickets gene locusM J Econs, P S Rowe, F Francis, et al.Genome Research|July 19, 2000
Characterization and repeat analysis of the compact genome of the freshwater pufferfish Tetraodon nigroviridisH Roest Crollius, O Jaillon, C Dasilva, et al.Human Molecular Genetics|August 1, 1994
A calcium channel mutation causing hypokalemic periodic paralysisK Jurkat-Rott, F Lehmann-Horn, A Elbaz, et al.Physiological Genomics|November 18, 2010
Atlas of gene expression in the mouse kidney: new features of glomerular parietal cellsLydie Cheval, Fabien Pierrat, Carole Dossat, et al.American Journal of Human Genetics|September 1, 1996
Genetic and physical mapping of the Chediak-Higashi syndrome on chromosome 1q42-43F J Barrat, L Auloge, E Pastural, et al.Pageof 46