Rossiter, B.J.F., Grompe, M., and Caskey, C.T. 
1991- Detection of deletions and point muta- 
tions. In PCR: A Practical Approach ( McPherson, 
M.J., Quirke, P., and Taylor, G.R., Eds.). Oxford, 
UK: Oxford University' Press, pp 67-83. 
Articles 
Bies, R.D., Friedman, D., Roberts, R., Perryman, 
M.B., and Caskey, C.T. 1992. Expression and lo- 
calization of dystrophin in human cardiac Pur- 
kinje fibers. Circulation 86:147-153- 
Bies, R.D., Phelps, S.F., Cortez, M.D., Roberts, R., 
Caskey, C.T., and Chamberlain, J.S. 1992. Hu- 
man and murine dystrophin mRNA transcripts are 
differentially expressed during skeletal muscle, 
heart, and brain development. Nucleic Acids Res 
20:1725-1731. 
Caskey, C.T. 1991 . Comments on DNA-based forensic 
analysis [letter]. Am J Hum Genet 4,9:^9^-^9'^ . 
Caskey, C.T. 1991. Physician-laboratory interface 
in X-chromosome mapping. Hosp Pract 26: 131- 
144. 
Caskey, C.T., Pizzuti, A., Fu, Y.-H., Fenwick, R.G., 
Jr., and Nelson, D.L. 1992. Triplet repeat muta- 
tions in human disease. Science 256:784-789. 
Caskey, C.T., and Rossiter, B.J.F. 1992. The human 
genome project. Purpose and potential. /P^arm 
Pharmacol (Suppl 1): 198-204. 
Caskey, C.T., and Rossiter, B.J.F. 1992. 9th Ernst 
Klenk Lecture. Molecular medicine. Biol Chem 
Hoppe Seyler 373:159-170. 
Chamberlain, J.S. , Chamberlain, J. R., Fenwick, R.G., 
Jr., Ward, P.A., Caskey, C.T., Dimnik, L.S., Bech- 
Hansen, N.T., Hoar, D.I., Tantravahi, U., Richards, 
S., Covone, A.E., Romeo, G., Abbs, S., Bentley, 
D.R., Bobrow, M., Rysiecki, G., Ray, P.N., 
Boileau, C, Junien, C, Boehm, C, Venne, V.L., 
Fujimura, F.K.. Spiga, I., Ferrari, M., Tedeschi, S., 
Bakker, E., Kneppers, A.L.J. , van Ommen, G.-J.B., 
Jain, K., Spector, E., Crandall, B., Kiuru, A., and 
Savontaus, M.-L. 1992. Diagnosis of Duchenne 
and Becker muscular dystrophies by polymer- 
ase chain reaction. A multicenter study. JAMA 
267:2609-2615. 
Chamberlain, J.S. , Farwell, N.J., Chamberlain, J. R., 
Cox, G.A., and Caskey, C.T. 1991. PCR analysis 
of dystrophin gene mutation and expression. / 
Cell Biochem 46:255-259. 
Clemens, P.R., Fenvv^ick, R.G., Chamberlain, J.S., 
Gibbs, R.A., de Andrade, M., Chakraborty, R., and 
Caskey, C.T. 1991- Carrier detection and prena- 
tal diagnosis in Duchenne and Becker muscular 
dystrophy families, using dinucleotide repeat 
polymorphisms. Am J Hum Genet 49:951-960. 
Cournoyer, D., Scarpa, M., Mitani, K., Moore, K.A., 
Markowitz, D., Bank, A., Belmont, J.W., and Cas- 
key, C.T. 1991. Gene transfer of adenosine deami- 
nase into primitive human hematopoietic progen- 
itor cells. Hum Gene Ther 2:203-213. 
Edwards, A., and Caskey, C.T. 1991 ■ Closure strate- 
gies for random DNA sequencing. Methods 3:41- 
47. 
Edwards, A., and Caskey, C.T. 1991. Genetic 
marker technology. Curr Opin Biotech 2:818- 
822. 
Edwards, A., Civitello, A., Hammond, H.A., and Cas- 
key, C.T. 1991. DNA raping and genetic mapping 
with trimeric and tetrameric tandem repeats. Am 
J Hum Genet 49:746-756. 
Edwards, A., Hammond, H.A., Jin, L., Caskey, C.T., 
and Chakraborty, R. 1992. Genetic variation at 
five trimeric and tetrameric tandem repeat loci in 
four human population groups. Genomics 12: 
241-253. 
Fu, Y.-H., Kuhl, D.P.A., Pizzuti, A., Pieretti, M., Sut- 
cliffe, J.S., Richards, S., Verkerk, A.J.M.H., Hol- 
den, J.J.A., Fenwick, R.G., Jr., Warren, S.T., Oos- 
tra, B.A., Nelson, D.L., and Caskey, C.T. 1991. 
Variation of the CGG repeat at the fragile X site 
results in genetic instability: resolution of the 
Sherman paradox. Cell 67:1047-1058. 
Fu, Y.-H., Pizzuti, A., Fenwick, R.G., Jr., King, J., 
Rajnarayan, S., Dunne, P.W., Dubel, J., Nasser, 
G.A., Ashizawa, T., de Jong, P., Wieringa, B., Kor- 
neluk, R., Ferryman, M.B., Epstein, H.F., and Cas- 
key, C.T. 1992. An unstable triplet repeat in a 
gene related to myotonic muscular dystrophy. 
Science 255:1256-1258. 
Gordon, R.B.. Dawson, P.A., Sculley, D.G., Emmer- 
son, B.T., Caskey, C.T., and Gibbs, R.A. 1991. 
The molecular characterisation of HPRTchermside 
and HPRTcoorparoo^ rwo Lesch-Nyhan patients 
with reduced amounts of mRNA Gene 108:299- 
304. 
Grompe, M., Jones, S.N., Loulseged, H., and Cas- 
key, C.T. 1992. Retroviral-mediated gene 
transfer of human ornithine transcarbamylase into 
primary hepatocytes of spf and spf-ash mice. 
Hum Gene Ther 5-55-44. 
Grompe. M., Pieretti, M., Caskey, C.T., and Balla- 
bio, A. 1992. The sulfatase gene family: cross- 
species PCR cloning using the MOPAC technique. 
Genomics 12:755-760. 
Grompe, M., Rao, N., Elder, F E B., Caskey, C.T., 
and Greenberg, F. 1992. 45,X/46,X,+r(X) can 
have a distinct phenot}'pe different from Ullrich- 
Turner syndrome. Am J Med Genet 42:59-45- 
Huang, T.H.-M., Hejtmancik, J.F., Edwards, A., Petti- 
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