Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5588975 | European Journal of Medical Genetics | 2017 | 38 Pages |
Abstract
Imprinting disorders as a group have characteristics that challenge diagnosis and management, including clinical and molecular heterogeneity, overlapping clinical features, somatic mosaicism, and multi-locus involvement. New insights into the biology and epigenomics of the early embryo offers new clues about the origin and importance of imprinting disorders.
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Authors
Deborah J.G. Mackay, I. Karen Temple,