Temple syndrome as a result of isolated hypomethylation of the 14q32 imprinted DLK1/MEG3 region. [electronic resource]
Producer: 20161019Description: 170-5 p. digitalISSN:- 1552-4833
- Abnormalities, Multiple -- genetics
- Adolescent
- Calcium-Binding Proteins
- Chromosomes, Human, Pair 14 -- genetics
- DNA Methylation -- genetics
- Developmental Disabilities -- genetics
- Female
- Genomic Imprinting -- genetics
- Humans
- Intercellular Signaling Peptides and Proteins -- genetics
- Membrane Proteins -- genetics
- Phenotype
- RNA, Long Noncoding -- genetics
- Uniparental Disomy -- genetics
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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