GENETIC AND BEHAVIOURAL ASPECTS OF PRADER-WILLI SYNDROME: A REVIEW WITH A TRANSLATION OF THE ORIGINAL PAPER

This publication has 39 references indexed in Scilit:

• Functional imprinting and epigenetic modification of the human SNRPN gene
  Human Molecular Genetics, 1993
• Frequent occurrence of translocations of the short arm of chromosome 15 to other D-group chromosomes
  Human Genetics, 1991
• Maternal origin of 15q11–13 deletions in Angelman syndrome suggests a role for genomic imprinting
  American Journal of Medical Genetics, 1990
• The association of Angelman's syndrome with deletions within 15q11-13.
  Journal of Medical Genetics, 1989
• Emotional symptoms in Prader‐Willi syndrome adolescents
  American Journal of Medical Genetics, 1987
• Abnormalities of the Central Visual Pathways in Prader–Willi Syndrome Associated with Hypopigmentation
  New England Journal of Medicine, 1986
• Neuropsychological capacity of prader-willi children: General and specific aspects of impairment
  Applied Research in Mental Retardation, 1986
• Prader-Willi Syndrome after age 15 years.
  Archives of Disease in Childhood, 1981
• Deletions of Chromosome 15 as a Cause of the Prader–Willi Syndrome
  New England Journal of Medicine, 1981
• Prader-Willi syndrome: A resumé of 32 cases including an instance of affected first cousins,one of whom is of normal stature and intelligence
  The Journal of Pediatrics, 1972