Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints. [electronic resource]
Producer: 19990820Description: 370-86 p. digitalISSN:- 0002-9297
- Angelman Syndrome -- genetics
- Animals
- Cell Line
- Chromosome Breakage -- genetics
- Chromosome Deletion
- Chromosomes, Human, Pair 15 -- genetics
- Cloning, Molecular
- Contig Mapping
- Female
- GTP-Binding Proteins -- genetics
- Gene Duplication
- Germ Cells -- metabolism
- Guanine Nucleotide Exchange Factors
- Humans
- Hybrid Cells
- In Situ Hybridization, Fluorescence
- Male
- Molecular Sequence Data
- Multigene Family
- Prader-Willi Syndrome -- genetics
- RNA, Messenger -- analysis
- Recombination, Genetic -- genetics
- Repetitive Sequences, Nucleic Acid -- genetics
- Transcription, Genetic -- genetics
- Ubiquitin-Protein Ligases
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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