Normal human genomic restriction-fragment patterns and polymorphisms revealed by hybridization with the entire dystrophin cDNA.

Eitemau Tebyg

• Myopathy in complex glycerol kinase deficiency patients is due to 3' deletions of the dystrophin gene.
  gan: Darras, B T, et al.
  Cyhoeddwyd: (1988)
• Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations.
  gan: Darras, B T, et al.
  Cyhoeddwyd: (1988)
• Regional assignment of six polymorphic DNA sequences on chromosome 21 by in situ hybridization to normal and rearranged chromosomes.
  gan: Münke, M, et al.
  Cyhoeddwyd: (1988)
• Analysis of restriction fragment length polymorphism in lymphokine genes of normal and autoimmune mice
  Cyhoeddwyd: (1989)
• Description of the entire mRNA population by a 3' end cDNA fragment generated by class IIS restriction enzymes.
  gan: Kato, K
  Cyhoeddwyd: (1995)