Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome. [electronic resource]
Producer: 20041004Description: 958-60 p. digitalISSN:- 1061-4036
- Alleles
- Beckwith-Wiedemann Syndrome -- genetics
- CCCTC-Binding Factor
- DNA Methylation
- DNA-Binding Proteins -- genetics
- Gene Deletion
- Gene Silencing
- Genomic Imprinting
- Humans
- Insulin-Like Growth Factor II -- genetics
- Molecular Sequence Data
- Pedigree
- RNA, Long Noncoding
- RNA, Untranslated
- Repressor Proteins -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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