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Pigment Cell Research|July 8, 2000
The use of expression profiling to study pigment cell biology and dysfunctionS K Loftus, W J PavanGenomics|July 20, 1995
Isolation, characterization, and precise physical localization of human CDX1, a caudal-type homeobox geneC A Bonner, S K Loftus, J J WasmuthGenome Research|January 1, 1996
Transcriptional map of the Treacher Collins candidate gene regionS K Loftus, J Dixon, K Koprivnikar, et al.Genomics|March 15, 1996
Genomic organization of the human heparan sulfate-N-deacetylase/N-sulfotransferase gene: exclusion from a causative role in the pathogenesis of Treacher Collins syndromeA J Gladwin, J Dixon, S K Loftus, et al.DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|January 5, 2002
Generation of RCAS vectors useful for functional genomic analysesS K Loftus, D M Larson, D Watkins-Chow, et al.Cytogenetics and Cell Genetics|January 1, 1994
Genes encoding adrenergic receptors are not clustered on the long arm of human chromosome 5S K Loftus, R Shiang, J A Warrington, et al.Genomics|March 20, 1995
Cloning of the human heparan sulfate-N-deacetylase/N-sulfotransferase gene from the Treacher Collins syndrome candidate region at 5q32-q33.1J Dixon, S K Loftus, A J Gladwin, et al.Human Molecular Genetics|November 1, 1993
A combined genetic and radiation hybrid map surrounding the Treacher Collins syndrome locus on chromosome 5qS K Loftus, S J Edwards, T Scherpbier-Heddema, et al.Human Molecular Genetics|October 1, 1996
Treacher Collins syndrome may result from insertions, deletions or splicing mutations, which introduce a termination codon into the geneA J Gladwin, J Dixon, S K Loftus, et al.American Journal of Human Genetics|August 1, 1994
A YAC contig encompassing the Treacher Collins syndrome critical region at 5q31.3-32J Dixon, A J Gladwin, S K Loftus, et al.Pageof 2