Hypopigmentation in Angelman syndrome

This publication has 17 references indexed in Scilit:

• An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome
  Nature, 1992
• Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene
  Nature, 1992
• Comparison of the 15q deletions in Prader‐Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences
  American Journal of Medical Genetics, 1990
• Biology of hypopigmentation
  Journal of the American Academy of Dermatology, 1988
• Molecular basis for the heterogeneity of human tyrosinase.
  The Tohoku Journal of Experimental Medicine, 1988
• Cloning and sequencing of mouse tyrosinase cDNA.
  The Japanese Journal of Genetics, 1987
• Abnormalities of the Central Visual Pathways in Prader–Willi Syndrome Associated with Hypopigmentation
  New England Journal of Medicine, 1986
• Hairbulb tyrosinase activity in oculocutaneous albinism: Suggestions for pathway control and block location
  American Journal of Medical Genetics, 1985
• The Angelman (“Happy Puppet”) syndrome
  American Journal of Medical Genetics, 1982
• ‘Puppet’ Children A Report on Three Cases
  Developmental Medicine and Child Neurology, 1965