Prenatal Diagnosis of Oculocutaneous Albinism by Analysis of the Fetal Tyrosinase Gene

This publication has 12 references indexed in Scilit:

• Molecular basis of type I (tryrosinase-related) oculocutaneous albinism: Mutations and polymorphisms of the human tyrosinase gene
  Human Mutation, 1993
• Do pigmented naevi in albinism provide evidence of tyrosinase positivity?
  British Journal of Dermatology, 1992
• A non-radioactive method for the detection of a common mutant allele of aldehyde dehydrogenase 2
  Molecular and Cellular Probes, 1992
• Detection of the most common mutation of adenine phosphoribosyltransferase deficiency among Japanese by a non-radioactive method
  Clinica Chimica Acta; International Journal of Clinical Chemistry, 1991
• Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene
  Biochemical and Biophysical Research Communications, 1989
• Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase
  Science, 1988
• PRENATAL DIAGNOSIS OF HEREDITARY SKIN DISORDERS
  Clinical Obstetrics and Gynecology, 1981
• Albinism in Nigeria1
  British Journal of Dermatology, 1975
• Skin Cancer in the South African Bantu
  British Journal of Cancer, 1953
• The Croonian Lectures ON INBORN ERRORS OF METABOLISM.
  The Lancet, 1908