Congenital adrenal hypoplasia, glycerol kinase deficiency and myopathy: condition requiring prompt identification. Clinical and biochemical findings in two cases

Gelijkaardige items

• Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: Molecular genetic evidence for deletions
  door: Francke, Uta, et al.
  Gepubliceerd in: (1987)
• Congenital adrenal hypoplasia and gonadotrophin deficiency.
  door: Black, S, et al.
  Gepubliceerd in: (1977)
• Congenital Adrenal Hypoplasia
  door: Cox, P J N
  Gepubliceerd in: (1962)
• 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.
  door: McCabe, E R, et al.
  Gepubliceerd in: (1989)
• Familial congenital adrenal hypoplasia.
  door: Uttley, W. S.
  Gepubliceerd in: (1968)