Angelman syndrome assessed by neurological and molecular cytogenetic investigations
- 31 January 1997
- journal article
- Published by Elsevier in Pediatric Neurology
- Vol. 16 (1) , 17-22
- https://doi.org/10.1016/s0887-8994(96)00264-0
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- On the prevalence of Angelman syndromeAmerican Journal of Medical Genetics, 1995
- Clinical profile of Angelman syndrome at different agesAmerican Journal of Medical Genetics, 1995
- Angelman syndrome: Consensus for diagnostic criteriaAmerican Journal of Medical Genetics, 1995
- Precocious puberty in a case with probable Angelman syndromeBrain & Development, 1994
- Maternal imprinting of human SNRPN, a gene deleted in Prader–Willi syndromeNature Genetics, 1994
- Characterization of a methylation imprint in the Prader — Willi syndrome chromosome regionHuman Molecular Genetics, 1993
- Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: An overviewAmerican Journal of Medical Genetics, 1993
- Exclusion of the GABAA-receptor β3 subunit gene as the Angelman's syndrome geneThe Lancet, 1993
- Incidence of 15q deletions in the Angelman syndrome: A survey of twelve affected personsAmerican Journal of Medical Genetics, 1989
- ‘Puppet’ Children A Report on Three CasesDevelopmental Medicine and Child Neurology, 1965