Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor β3-subunit gene
- 8 February 1992
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 339 (8789), 366-367
- https://doi.org/10.1016/0140-6736(92)91686-3
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- DNA deletion and its parental origin in Angelman syndrome patientsAmerican Journal of Medical Genetics, 1991
- Uniparental paternal disomy in Angelman's syndromeThe Lancet, 1991
- Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndromeNature, 1989
- Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletionAmerican Journal of Medical Genetics, 1989