On the parental origin of the deletion in Angelman syndrome

This publication has 5 references indexed in Scilit:

• Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader‐Willi syndrome
  American Journal of Medical Genetics, 1989
• Detection of a 15q deletion in a child with Angelman syndrome by cytogenetic analysis and flow cytometry
  American Journal of Medical Genetics, 1989
• Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion
  American Journal of Medical Genetics, 1989
• Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes
  Human Genetics, 1988
• Clinical heterogeneity associated with deletions in the long arm of chromosome 15: Report of 3 new cases and their possible genetic significance
  American Journal of Medical Genetics, 1987