PRENATAL DIAGNOSIS OF CLASSIC PHENYLKETONURIA BY DNA ANALYSIS

This publication has 9 references indexed in Scilit:

• Detection of specific sequences among DNA fragments separated by gel electrophoresis
  Published by Elsevier ,2006
• Phenylketonuria: 50 Years since Felling's Discovery and still Expanding our Clinical and Biochemical Knowledge
  Acta Paediatrica, 1984
• Prenatal diagnosis of classical phenylketonuria by gene mapping
  Published by American Medical Association (AMA) ,1984
• Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria
  Nature, 1983
• Phenylketonuria: Epitome of Human Biochemical Genetics
  New England Journal of Medicine, 1980
• Nucleotide sequence of the rightward operator of phage lambda.
  Proceedings of the National Academy of Sciences, 1975
• Preliminary Communication
  The Lancet, 1953
• PHENYLPYRUVIC OLIGOPHRENIA DEFICIENCY OF PHENYLALANINE-OXIDIZING SYSTEM
  1953
• Über Ausscheidung von Phenylbrenztraubensäure in den Harn als Stoffwechselanomalie in Verbindung mit Imbezillität.
  Hoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1934