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- W1575296735 endingPage "175" @default.
- W1575296735 startingPage "145" @default.
- W1575296735 abstract "Genomic imprinting represents a form of epigenetic control of gene expression in which one allele of a gene is preferentially expressed according to the parent-of-origin of the allele. Genomic imprinting plays an important role in normal growth and development. Disruption of imprinting can result in a number of human imprinting syndromes and predispose to cancer. In this chapter, we describe a number of human imprinting syndromes to illustrate the concepts of genomic imprinting and how loss of imprinting of imprinted genes their relationship to human neoplasia." @default.
- W1575296735 created "2016-06-24" @default.
- W1575296735 creator A5033933023 @default.
- W1575296735 creator A5056034710 @default.
- W1575296735 date "2010-01-01" @default.
- W1575296735 modified "2023-09-24" @default.
- W1575296735 title "Genomic Imprinting Syndromes and Cancer" @default.
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