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Annals of Tropical Paediatrics
International Child Health
Volume 13, 1993 - Issue 1
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Original Articles

Deletion screening of Sri Lankan Duchenne muscular dystrophy patients using the polymerase chain reaction

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Pages 83-86 | Received 09 Dec 1991, Published online: 13 Jul 2016

References

  • Koenig M, Beggs AH, Moyer M, et al. The molecular basis for Duchenne versus Becker muscular dystrophy: Correlation of severity with type of deletion. Am J Hum Genet 1989; 45: 4948–56.
  • Liechti-Gallati S, Koenig M, Kunkel LM, et al. Molecular deletion patterns in Duchenne and Becker type muscular dystrophy. Hum Genet 1989; 81: 343–8.
  • Hoffman EP, Fischbeck KH, Brown RH, et al. Characterization of dystrophin in muscle biopsy specimens from patients with Duchenne and Becker muscular dystrophy. N Engl J Med 1988; 318: 1363–8.
  • Forrest SM, Cross GS, Speer A, Gardner-Medwin D, Davies KE. Preferential deletion of exons in Duchenne and Becker muscular dystrophies. Nature (London) 1987; 329: 638–40.
  • Gillard EF, Chamberlain JS, Murphy EG, et al. Molecular and phenotypic analysis of patients with deletions within the deletion rich region of the Duchenne Muscular Dystrophy (DMD) gene. Am J Hum Genet 1989; 45: 507–20.
  • White TJ, Arnheim N, Erlich HA. The polymerase chain reaction. Trends Genet 1989; 5: 185–9.
  • Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucl Acid Res 1988; 16: 1215.
  • Chamberlain JS, Gibbs RA, Rainer JH, Nguyen PN, Caskey CT. Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification. Nucl Acid Res 1988; 16: 1141–56.

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