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A rare MspI RFLP of the DMD probe p20 (DXS269)

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Summary

A rare polymorphism of the probe p20 in the Duchenne muscular dystrophy gene is reported.

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References

  • Murray JM, Davies KE, Harper PS, Meredith L, Mueller CR, Williamson R (1982) Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne uscular dystrophy. Nature (London) 300:69–71

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  • Wapenaar MC, Kievits T, Hart KA, Abbs S, Blonden LAJ, Dunnen JT den, Grootscholten PM, Bakker E, Verellen-Dumoulin C, Bobrow M, Ommen GJB van, Pearson PL (1988) A deletion hot spot in the Duchenne muscular dystrophy gene. Genomics 2:101–108

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Authors and Affiliations

  1. Institut für Humangenetik der Universität, Wilhelmstrasse 31, W-5300, 1, Bonn, Federal Republic of Germany

    S. Uhlhaas & W. Friedl

  2. Department of Human Genetics, Leiden University, Sylvius Laboratory, Wassenaarseweg 72, NL-2333, AL Leiden, The Netherlands

    E. Bakker

  3. Department of Biochemistry, University of Antwerp, Universiteitsplein 1, B-2610, Wilrijk, Belgium

    C. van Broeckhoven

  4. Institut für Humangenetik der Universität, Theodor-Stern-Kai 7, W-6000, 70, Frankfurt/M, Federal Republic of Germany

    A. Barth-Schulz

Authors
  1. S. Uhlhaas
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  2. E. Bakker
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  3. C. van Broeckhoven
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  4. A. Barth-Schulz
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  5. W. Friedl
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Uhlhaas, S., Bakker, E., van Broeckhoven, C. et al. A rare MspI RFLP of the DMD probe p20 (DXS269). Hum Genet 89, 122 (1992). https://doi.org/10.1007/BF00207060

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  • DOI: https://doi.org/10.1007/BF00207060

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