The GABAA receptor beta 3 subunit gene: characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7 (Q24321885)

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English	The GABAA receptor beta 3 subunit gene: characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7	scientific article

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The GABAA receptor beta 3 subunit gene: characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7 (English)

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author name string

J Wagstaff

1

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J R Chaillet

2

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M Lalande

3

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language of work or name

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publication date

December 1991

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11

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1071-8

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4

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Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance.

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Is Angelman syndrome an alternate result of del(15)(q11q13)?

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https://api.crossref.org/works/10.1016%2F0888-7543%2891%2990034-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

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https://api.crossref.org/works/10.1016%2F0888-7543%2891%2990034-C

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Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome

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A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

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Phylogenetic receptor research: implications in studying psychiatric and neurological disease

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The syntenic relationship between the critical deletion region for the Prader-Willi/Angelman syndromes and proximal mouse chromosome 7

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Isolation, characterization, and localization of human genomic DNA encoding the β1 subunit of the GABAA receptor (GABRB1)

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Chromosomal localization of GABAA receptor subunit genes: relationship to human genetic disease.

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Cyclic AMP-dependent protein kinase decreases GABAA receptor current in mouse spinal neurons

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Parental origin of chromosome 15 deletion in Prader-Willi syndrome

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https://api.crossref.org/works/10.1016%2F0888-7543%2891%2990034-C

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Genome imprinting phenomena on mouse chromosome 7

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Sequence and functional expression of the GABA A receptor shows a ligand-gated receptor super-family.

1 reference

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Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

1 reference

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Deletions of chromosome 15 as a cause of the Prader-Willi syndrome

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7 January 2021

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The murine GABAA receptor delta-subunit gene: structure and assignment to human chromosome 1

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Sequence of the chicken GABAA receptor beta 3-subunit cDNA.

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Molecular biology of GABAA receptors

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GABAergic mechanisms in the pathogenesis and treatment of epilepsy

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‘Puppet’ Children A Report on Three Cases

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7 January 2021

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Identifiers

10.1016/0888-7543(91)90034-C

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