PUBLICATIONS 
Books and Chapters of Books 
Kunkel, L.M. 1989. Duchenne muscular dystrophy: identification of the gene. \n Molecular Genetics in Dis- 
eases of Brain, Nerve, and Muscle (Rowland, L.E, Wood, D.S., Schon, E.A., and DiMauro, S., Eds.). New 
York: Oxford University Press, pp 370-379. 
Articles 
Burmeister, M., Monaco, A.R, GiUard, E.F., van Ommen, G.J.B., Affara, N.A., Ferguson-Smith, M.A., Kunkel, 
L.M., and Lehrach, H. 1988. A 10-megabase physical map of human Xp21, including the Duchenne muscu- 
lar dystrophy gene. Genomics 2:189-202. 
Feener, C.A., Koenig, M., and Kunkel, L.M. 1989. Alternative splicing of human dystrophin mRNA generates 
isoforms at the carboxy terminus. Nature 338:509-511. 
Hoffman, E.P., and Kunkel, L.M. 1989. Dystrophin abnormalities in Duchenne/Becker muscular dystrophy 
Neuron 2:1019-1029. 
Hoffman, E.E, Kunkel, L.M., Angelini, C, Clarke, A., Johnson, M., and Harris, J. B. 1989. Improved diagnosis of 
Becker muscular dystrophy via dystrophin testing. Neurology 39:1011-1017. 
Hoffman, E.E, Watkins, S.C., Slayter, H.S., and Kunkel, L.M. 1989. Detection of a specific isoform of alpha- 
actinin with antisera directed against dystrophin./ Cell Biol 108:503-510. 
Hurko, O., Hoffman, E.E, McKee, L., Johns, D.R., and Kunkel, L.M. 1989. Dystrophin analysis in clonal 
myoblasts derived from a Duchenne muscular dystrophy carrier. Am J Hum Genet 44:820-826. 
Kunkel, L.M. 1989. Muscular dystrophy: a time of hope. Proc R Soc Lond B 237: 1-9. 
Kunkel, L.M., Beggs, A.H., and Hoffman, E.E 1989. Molecular genetics of Duchenne and Becker muscular 
dystrophy: emphasis on improved diagnosis. Clin Chem 35:B21-B24. 
Kunkel, L.M., and Hoffman, E.E 1989. Duchenne/Becker muscular dystrophy: a short overview of the gene, 
the protein, and current diagnostics. Br Med J 45:650-643. 
Kwan, S.-E, Sandkuyl, L.A., Blaese, M., Kunkel, L.M., Bruns, G., Earmley R., Skarshaug, S., Page, D.C., Ott, J., 
and Rosen, F.S. 1988. Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymor- 
phic DNA markers. Genomics 3:39-43. 
McCabe, E.R.B., Towbin, J., Chamberlain, J., Baumbach, L, Witkowski, J., van Ommen, GJ.B., Koenig, M. , 
Kunkel, L.M., and Seltzer, WK. 1989. Complementary DNA probes for the Duchenne muscular dystrophy 
locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol ki- 
nase deficiency, and congenital adrenal hypoplasia./ Clin Invest 83:95-99. 
Partridge, T.A., Morgan, J.E., Coulton, G.R., Hoffman, E.E, and Kunkel, L.M.. 1989. Conversion of mdx 
myofibres from dystrophin-negative to -positive by injection of normal myoblasts. Nature 337:176-179- 
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