Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.

Παρόμοια τεκμήρια

• Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy.
  ανά: Meredith, A L, κ.ά.
  Έκδοση: (1986)
• Gene deletions in X-linked muscular dystrophy
  ανά: Lindlöf, Mikael, κ.ά.
  Έκδοση: (1989)
• Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism.
  ανά: Kwan, S P, κ.ά.
  Έκδοση: (1986)
• The use of multiple restriction fragment length polymorphisms in prenatal risk estimation. I. X-linked diseases.
  ανά: Clark, A G
  Έκδοση: (1985)
• Detection of carriers of benign X-linked muscular dystrophy.
  ανά: Emery, A E, κ.ά.
  Έκδοση: (1967)