An animal model for maternal phenylketonuria.

Ítems similars

• Single-strand conformation polymorphism for detection of mutations and base substitutions in phenylketonuria.
  per: Labrune, P, et al.
  Publicat: (1991)
• Two distinct mutations at a single BamHI site in phenylketonuria.
  per: Melle, D, et al.
  Publicat: (1991)
• Genetic background of clinical homogeneity of phenylketonuria in Poland.
  per: Jaruzelska, J, et al.
  Publicat: (1993)
• Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency.
  per: Lyonnet, S, et al.
  Publicat: (1989)
• Maternal phenylketonuria.
  per: Farquhar, J W, et al.
  Publicat: (1971)