Complementary DNA probes for the Duchenne muscular dystrophy locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasia.

Ítems similars

• Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: Molecular genetic evidence for deletions
  per: Francke, Uta, et al.
  Publicat: (1987)
• The Non-Dystrophic Myopathies
  per: Pearce, John
  Publicat: (1965)
• Deletion mapping of Aland Island eye disease to Xp21 between DXS67 (B24) and Duchenne muscular dystrophy.
  per: Pillers, D A, et al.
  Publicat: (1990)
• Congenital adrenal hypoplasia, glycerol kinase deficiency and myopathy: condition requiring prompt identification. Clinical and biochemical findings in two cases
  per: Vasanwala, Rashida, et al.
  Publicat: (2013)
• Experience of observing patients with Duchenne myopathy
  per: L. I. Minaycheva, et al.
  Publicat: (2023-12-01)