The GABAA receptor β3 subunit gene: Characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7
- 31 December 1991
- Vol. 11 (4) , 1071-1078
- https://doi.org/10.1016/0888-7543(91)90034-c
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- PARENTAL ORIGIN OF CHROMOSOME 15 DELETION IN PRADER-WILLI SYNDROMEThe Lancet, 2003
- The syntenic relationship between the critical deletion region for the Prader-Willi/Angelman syndromes and proximal mouse chromosome 7Genomics, 1991
- Isolation, characterization, and localization of human genomic DNA encoding the β1 subunit of the GABAA receptor (GABRB1)Genomics, 1991
- Sequence of the chicken GABAAreceptor β3-subunit cDNANucleic Acids Research, 1990
- Chromosomal localization of GABAA receptor subunit genes: relationship to human genetic diseaseNeuron, 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
- Phylogenetic receptor research: Implications in studying psychiatric and neurological diseaseJournal of Psychiatric Research, 1987
- Clinical heterogeneity associated with deletions in the long arm of chromosome 15: Report of 3 new cases and their possible genetic significanceAmerican Journal of Medical Genetics, 1987
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityAnalytical Biochemistry, 1983
- ‘Puppet’ Children A Report on Three CasesDevelopmental Medicine and Child Neurology, 1965