Fletcher, F.A., Moore, K.A., MacGregor, G.R., Belmont, J.W, and Caskey, C.T. 1988. Human gene expression in 
murine hemopoietic cells in vivo. In Molecular Biology of Hemopoiesis (Tavassoli, M., Zanjani, E.D., As- 
censao, J.L., Abraham, N.G., and Levine, A.S., Eds.). New York: Plenum, vol 241, pp 123-127. 
Gibbs, R.A., Chamberlain, J.S., and Caskey, C.T. 1989. Diagnosis of new mutation diseases using the polymer- 
ase chain reaction. In PCR Technology: Principles and Applications of DNA Amplification (Erlich, H.A., 
Ed.). New York: Stockton, pp 171-191. 
Gibbs, R.A., Patel, PL, Stout, J.T., and Caskey, C.T. 1989. Lesch-Nyhan syndrome: human hypoxanthine phos- 
phoribosyl transferase deficiency. In Molecular Genetics in Diseases of Brain, Nerve, and Muscle (Row- 
land, LP, Wood, D.S., Schon, E.A., and DiMauro, S., Eds.). New York: Oxford University Press, pp 211-220. 
Hejtmancik, J.F., Witkowski, J., Gunnel, S., Davis, S., Baumbach, L., Ward, P, and Caskey, C.T. 1988. Prenatal 
and carrier detection of Duchenne muscular dystrophy using recombinant DNA technology. In Nucleic 
Acid Probes in Diagnosis of Human Genetic Diseases (Willey, A.M., Ed.). New York: Liss, pp 83-100. 
Lupski, J.R., and Caskey, C.T. 1989. Molecular mechanisms and detection of mutations leading to human dis- 
ease phenotypes. \n Molecular Genetics of Brain, Nerve, and Muscle (Rowland, L.P, Wood, D.S., Schon, 
E.A., and DiMauro, S., Eds.). New York: Oxford University Press, pp 102-122. 
MacGregor, G.R., Nelson, D.L., Chang, S.M.W, and Caskey, C.T. 1989. Gene replacement therapy: the exam- 
ple of Lesch-Nyhan syndrome. In Molecular Genetics of Diseases of Brain, Nerve, and Muscle (Rowland, 
LP, Wood, D.S., Schon, E.A., and DiMauro, S., Eds.). New York: Oxford University Press, pp 417-425. 
Stout, J.T, and Caskey, C.T. 1989. Hypoxanthine phosphoribosyltransferase deficiency: the Lesch-Nyhan syn- 
drome and gouty arthritis. In The Metabolic Basis of Inherited Disease (Scriver, C.R., Beaudet, A.L., Sly, 
WS., and Valle, D. , Eds.). New York: McGraw-Hill, pp 1007-1028. 
Articles 
Baumbach, L.L., Chamberlain, J. S., Ward, PA., Farwell, N.J., and Caskey, C.T. 1989. Molecular and clinical cor- 
relations of deletions leading to Duchenne and Becker muscular dystrophies. Neurology 39:465-474. 
Belmont, J.W, MacGregor, G.R., Wager-Smith, K. , Fletcher, F.A., Moore, K.A., Hawkins, D. , Villalon, D., Chang, 
S.M.-W, and Caskey, C.T. 1988. Expression of human adenosine deaminase in murine hematopoietic cells. 
Mol Cell Biol 8:5116-512 5 . 
Chamberlain, J.S., Gibbs, R.A., Ranier, J.E., Nguyen, P.-N., and Caskey, C.T. 1988. Deletion screening of the 
Duchenne muscular dystrophy locus via multiplex DNA amplification. Nucleic Acids Res 16:11141-11156. 
Chapman, VM., Miller, D.R., Armstrong, D., and Caskey, C.T 1989. Recovery of induced mutations for X chro- 
mosome-linked muscular dystrophy in mice. Proc Natl Acad Sci USA 86:1292-1296. 
Chen, J. D., Hejtmancik, J. F., Romeo, G., Linklof, M., Boehm, C, Caskey, C.T, Kress, W, Fishbeck, K.H., Drier, 
M., Serravalle, S., Grimm, T, Kaariainen, H., Ferrari, M., Pfendner, E., Meng, G., de la Chapelle, A., Melis, 
M.A., MuUer, B., Mackinlay, A.G., Mueller, C.R., and Denton, M.J. 1989- A genetic linkage map of five 
marker loci in and around the Duchenne muscular dystrophy locus. Genomics 4:105-109. 
Gibbs, R.A., and Caskey, C.T. 1989. The application of recombinant DNA technology for genetic probing in 
epidemiology. Annu Rev Public Health 10:27-48. 
Gibbs, R.A., Nguyen, P-N., and Caskey, C.T. 1989. Detection of single DNA base differences by competitive oli- 
gonucleotide pnmin%. Nucleic Acids Res 17:2437-2448. 
Gibbs, R.A., Nguyen, P-N. , McBride, LJ., Koepf, S.M., and Caskey, C.T. 1989. Identification of mutations lead- 
ing to the Lesch-Nyhan syndrome by automated direct DNA sequencing of in vitro amplified cDNA. Proc 
Natl Acad Sci USA 86:1919-1923. 
Grompe, M., Muzny, D.M., and Caskey, C.T. 1989. Scanning detection of mutations in human ornithine trans- 
carbamylase by chemical mismatch cleavage. Proc Natl Acad Sci USA 86:5888-5892. 
Hofftnan, E.P, Fischbeck, K., Brown, R.H., Johnson, M., Medori, R., Loike, J.D., Harris, J.B., Waterston, R., 
Brook, M., Specht, L., Kupsky, R., Chamberlain, J. S., Caskey, C.T , Shapiro, F., and Kunkel, L.M. 1988. Char- 
acterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscu- 
lar dystrophy. N Engl f Med 318:1363-1368. 
Continued 
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