Angelman syndrome: a review of clinical and genetic aspects
- 1 September 1999
- journal article
- review article
- Published by Elsevier in Clinical Neurology and Neurosurgery
- Vol. 101 (3) , 161-170
- https://doi.org/10.1016/s0303-8467(99)00030-x
Abstract
No abstract availableKeywords
This publication has 57 references indexed in Scilit:
- Uniparental Disomies in Unselected PopulationsAmerican Journal of Human Genetics, 1998
- De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndromeNature Genetics, 1997
- UBE3A/E6-AP mutations cause Angelman syndromeNature Genetics, 1997
- Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15Nature Genetics, 1995
- Modification of 15q11 — q13 DNA methylation imprints in unique Angelman and Prader — Willi patientsHuman Molecular Genetics, 1993
- Angelman Syndrome: Clinical ProfileJournal of Child Neurology, 1992
- DNA deletion and its parental origin in Angelman syndrome patientsAmerican Journal of Medical Genetics, 1991
- Incidence of 15q deletions in the Angelman syndrome: A survey of twelve affected personsAmerican Journal of Medical Genetics, 1989
- The association of Angelman's syndrome with deletions within 15q11-13.Journal of Medical Genetics, 1989
- Deletions of Chromosome 15 as a Cause of the Prader–Willi SyndromeNew England Journal of Medicine, 1981