Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31COFFEEN, C. M; MCKENNA, C. E; FU, Y.-H et al.Human molecular genetics (Print). 2000, Vol 9, Num 5, pp 787-793, issn 0964-6906Article

Newborn screening for cystic fibrosis in Wisconsin: Comparison of biochemical and molecular methodsGREGG, R. G; SIMANTEL, A; SPLAINGARD, M et al.Pediatrics (Evanston). 1997, Vol 99, Num 6, pp 819-824, issn 0031-4005Article

Localization of a non-specific X-linked mental retardation gene, MRX23, to Xq23-q24GREGG, R. G; PALMER, C; KIRKPATRICK, S et al.Human molecular genetics (Print). 1996, Vol 5, Num 3, pp 411-414, issn 0964-6906Article

Assignment of the human gene for the β subunit of the voltage-dependent calcium channel (CACNLB1) to chromosome 17 using somatic cell hybrids and linkage mappingGREGG, R. G; POWERS, P. A; HOGAN, K et al.Genomics (San Diego, Calif.). 1993, Vol 15, Num 1, pp 185-187, issn 0888-7543Article

Dinucleotide repeat polymorphism at the RYR1 locus (19q13.1)COUCH, F. J; HOGAN, K; MCCARTHY, T. V et al.Nucleic acids research. 1991, Vol 19, Num 18, issn 0305-1048, 5094Article

Structure and alternative splicing of the gene encoding the human β₁ subunit of voltage dependent calcium channelsHOGAN, K; GREGG, R. G; POWERS, P. A et al.Neuroscience letters. 1999, Vol 277, Num 2, pp 111-114, issn 0304-3940Article

Morphological and physiological consequences of the selective elimination of rod photoreceptors in transgenic miceMCCALL, M. A; GREGG, R. G; MERRIMAN, K et al.Experimental eye research. 1996, Vol 63, Num 1, pp 35-49, issn 0014-4835Article

The structure of the gene encoding the human skeletal muscle α₁ subunit of the dihydropyridine-sensitive L-type calcium channel (CACNL1A3)HOGAN, K; GREGG, R. G; POWERS, P. A et al.Genomics (San Diego, Calif.). 1996, Vol 31, Num 3, pp 392-394, issn 0888-7543Article

Dinucleotide repeat polymorphism at the D17S518 locusCOUCH, F. J; MCCARTHY, T. V; GREGG, R. G et al.Nucleic acids research. 1991, Vol 19, Num 18, issn 0305-1048, 5093Article

Hepatic cholesterol synthesis and hydroxymethylglutaryl CoA reductase activity after injection of methylazoxymethanol acetateGREGG, R. G; WILCE, P. A.Cancer biochemistry biophysics. 1987, Vol 9, Num 3, pp 281-287, issn 0305-7232Article

Application of DNA analysis in a population-screening program for neonatal diagnosis of cystic fibrosis (CF) : comparison of screening protocolsGREGG, R. G; WILFOND, B. S; FARRELL, P. M et al.American journal of human genetics. 1993, Vol 52, Num 3, pp 616-626, issn 0002-9297Article

G to A polymorphism in the CACNLG geneOLCKERS, A; JEDLICKA, A. E; POWERS, P. A et al.Human molecular genetics (Print). 1993, Vol 2, Num 12, issn 0964-6906, p. 2198Article

A cysteine-for-arginine substitution (R614C) in the human skeletal muscle calcium release channel cosegregates with malignant hyperthermiaHOGAN, K; COUCH, F; POWERS, P. A et al.Anesthesia and analgesia. 1992, Vol 75, Num 3, pp 441-448, issn 0003-2999Article

Assignment of the human gene for the α1 subunit of the cardiac DHP-sensitive Ca²⁺ channel (CCHL1A1) to chromosome 12p12-pterPOWERS, P. A; GREGG, R. G; LALLEY, P. A et al.Genomics (San Diego, Calif.). 1991, Vol 10, Num 3, pp 835-839, issn 0888-7543, 5 p.Article

Dinucleotide repeat polymorphism at the D8S161 locusCOUCH, F. J; MCCARTHY, T. V; GREGG, R. G et al.Nucleic acids research. 1991, Vol 19, Num 18, issn 0305-1048, 5093Article

Regulated expression of genes inserted at the human chromosomal β-globin locus by homologous recombinationNANDI, A. K; ROGINSKI, R. S; GREGG, R. G et al.Proceedings of the National Academy of Sciences of the United States of America. 1988, Vol 85, Num 11, pp 3845-3849, issn 0027-8424Article

Linkage mapping of the human gene for the α₁ subunit of the cardiac DHP-sensitive Ca²⁺ channel (CACNL1A1) to chromosome 12p13.2-pter using a dinucleotide repeatPOWERS, P. A; GREGG, R. G; HOGAN, K et al.Genomics (San Diego, Calif.). 1992, Vol 14, Num 1, pp 206-207, issn 0888-7543Article

Dinucleotide repeat polymorphism at the D7S547 locusGREGG, R. G; PARKER, M. B.Human molecular genetics (Print). 1992, Vol 1, Num 8, issn 0964-6906, p. 659Article

Localization of the mouse nob (no b-wave) gene to the centromeric region of the X chromosomeCANDILLE, S. I; PARDUE, M. T; MCCALL, M. A et al.Investigative ophthalmology & visual science. 1999, Vol 40, Num 11, pp 2748-2751, issn 0146-0404Article

Genetic heterogeneity in families with hereditary multiple exostosesCOOK, A; RASKIND, W; WIJSMAN, E et al.American journal of human genetics. 1993, Vol 53, Num 1, pp 71-79, issn 0002-9297Article

Skeletal muscle and brain isoforms of a β-subunit of human voltage-dependent calcium channels are encoded by a single genePOWERS, P. A; SHUYING LIU; HOGAN, K et al.The Journal of biological chemistry (Print). 1992, Vol 267, Num 32, pp 22967-22972, issn 0021-9258Article

Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: localization to Xq27.3-qterGREGG, R. G; METZENBERG, A. B; HOGAN, K et al.Genomics (San Diego, Calif.). 1991, Vol 9, Num 4, pp 701-706, issn 0888-7543, 6 p.Article

Regulatory elements in the introns of the human HPRT gene are necessary for its expression in embryonic stem cellsREID, L. H; GREGG, R. G; SMITHIES, O et al.Proceedings of the National Academy of Sciences of the United States of America. 1990, Vol 87, Num 11, pp 4299-4303, issn 0027-8424, 5 p.Article