Exclusion of the GABAA-receptor β3 subunit gene as the Angelman's syndrome gene
- 9 January 1993
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 341 (8837) , 122-123
- https://doi.org/10.1016/0140-6736(93)92606-t
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Dinucleotide repeat polymorphism at the D15S11 locus in the Angelman/Prader—Willi region (AS/PWS) of chromosome 15Human Molecular Genetics, 1992
- Dinucleotide repeat polymorphism at the GABAA receptor β3 (GABRB3) locus in the Angelman/Prader— Willi region (AS/PWS) of chromosome 15Human Molecular Genetics, 1992
- Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor β3-subunit geneThe Lancet, 1992
- DNA deletion and its parental origin in Angelman syndrome patientsAmerican Journal of Medical Genetics, 1991
- Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader‐Willi syndromeAmerican Journal of Medical Genetics, 1989
- The association of Angelman's syndrome with deletions within 15q11-13.Journal of Medical Genetics, 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