Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients

Ítems similars

• Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients
  per: Aziza Sbiti, et al.
  Publicat: (2002-01-01)
• Carrier Frequency of the c.525delT Mutation in the SGCG Gene and Estimated Prevalence of Limb Girdle Muscular Dystrophy Type 2C Among the Moroccan Population
  per: El Kerch, Fatiha, et al.
  Publicat: (2014)
• Screening Duchenne and Becker muscular dystrophy patients for deletions in 30 exons of the dystrophin gene by three-multiplex PCR.
  per: Covone, A E, et al.
  Publicat: (1992)
• Analysis of quantitative PCR for the diagnosis of deletion and duplication carriers in the dystrophin gene.
  per: Abbs, S, et al.
  Publicat: (1992)
• The use of a new multiplex PCR assay significantly improves the rapid detection of deletions in the dystrophin gene.
  per: Tarleton, J C, et al.
  Publicat: (1991)