New mutation and prenatal diagnosis in ornithine transcarbamylase deficiency.

Παρόμοια τεκμήρια

• Gene Mutation Analysis and Prenatal Diagnosis of the Ornithine Transcarbamylase (OTC) Gene in Two Families with Ornithine Transcarbamylase Deficiency
  ανά: Li, Sitao, κ.ά.
  Έκδοση: (2018)
• Characterization of point mutations in the same arginine codon in three unrelated patients with ornithine transcarbamylase deficiency.
  ανά: Maddalena, A, κ.ά.
  Έκδοση: (1988)
• Prenatal diagnosis of ornithine transcarbamylase deficiency utilizing fetal liver biopsy.
  ανά: Holzgreve, W, κ.ά.
  Έκδοση: (1984)
• Family studies in ornithine transcarbamylase deficiency.
  ανά: Svirklys, L G, κ.ά.
  Έκδοση: (1988)
• Site specific screening for point mutations in ornithine transcarbamylase deficiency.
  ανά: Feldmann, D, κ.ά.
  Έκδοση: (1992)