DNA deletions and recombinations in the gene locus of X-linked muscular dystrophies
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01800385
Reference15 articles.
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2. Bakker, E., Bonten, E. J., Delange, L. E., Veenema, H., Majoor-Krakauer, D., Hofker, M. H., van Ommen, G. J. B. and Pearson, P. L. DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: A standard diagnostic procedure.J. Med. Genet. 23 (1986) 573–580
3. Blin, N. and Stafford, D. E. A general method for isolation of high molecular weight DNA from eukaryotes.Nucleic Acids Res. 3 (1976) 2303–2308
4. Burghes, A. H. M., Logan, C., Hu, X., Belfall, B., Worton, R. G. and Ray, P. N. A cDNA clone from the Duchenne/Becker muscular dystrophy gene.Nature (London) 328 (1987) 434–437
5. Fischbeck, K. H., Ritter, A. W., Tirschwell, D. L., Kunkel, L. M., Bertelson, C. J., Monaco, A. P., Hejtmancik, J. F., Booen, C., Ionasescu, V., Ionasescu, R., Pericak-Vance, M., Kandt, R. and Roses, A. D. Recombination with pERT87 (DX164) in families with X-linked muscular dystrophy.Lancet 2 (1986) 104
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1. A screening for dystrophin gene deletions in Japanese patients with Duchenne/Becker muscular dystrophy by the multiplex polymerase chain reaction;Brain and Development;1991-09
2. Dystrophin immunohistochemistry in a symptomatic carrier of becker muscular dystrophy;Journal of Neurology;1991
3. Two-dimensional electrophoresis aided by personal computer analysis for screening of mutant proteins in inherited diseases;Electrophoresis;1989
4. Restriction fragment length polymorphisms on the short arm of X chromosome among the Japanese population;Japanese journal of human genetics;1988-09
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