Article
Prader-Willi and Angelman syndromes. Disorders of genomic imprinting.
Medicine - 1 Mar 1998
Cassidy S B, Schwartz S
Abstract excerpt
Prader-Willi and Angelman syndromes are 2 clinically distinct disorders associated with multiple anomalies and mental retardation. They are only discussed together because they share a similar and uncommon genetic basis: they involve genes that are located in the same region in the genome and are...
Topics
- Adult
- Angelman Syndrome
- Chromosome Deletion
- Chromosomes, Human, Pair 13
- Chromosomes, Human, Pair 15
- Female
- Genetic Counseling
- Genomic Imprinting
- Genotype
- Humans
- Male
- Phenotype
- Prader-Willi Syndrome
- Prenatal Diagnosis
- Risk Assessment
