Two human cDNA molecules coding for the Duchenne muscular dystrophy (DMD) locus are highly homologous.

Benzer Materyaller

• DNA amplification of a further exon of Duchenne muscular dystrophy locus increase possibilities for deletion screening.
  Yazar:: Speer, A, ve diğerleri
  Baskı/Yayın Bilgisi: (1989)
• Deletions of fetal and adult muscle cDNA in Duchenne and Becker muscular dystrophy patients.
  Yazar:: Cross, G S, ve diğerleri
  Baskı/Yayın Bilgisi: (1987)
• CUGC for Duchenne muscular dystrophy (DMD)
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  Baskı/Yayın Bilgisi: (2018)
• Symptomatic therapy of Duchenne Muscular Dystrophy (DMD)
  Yazar:: Rüdel, Reinhardt
  Baskı/Yayın Bilgisi: (2012)
• Possibilities and limitation of prenatal diagnosis and carrier determination for Duchenne and Becker muscular dystrophy using cDNA probes.
  Yazar:: Speer, A, ve diğerleri
  Baskı/Yayın Bilgisi: (1989)