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- W2124234443 endingPage "369" @default.
- W2124234443 startingPage "347" @default.
- W2124234443 abstract "Human imprinting disorders can provide critical insights into the role of imprinted genes in human development and health, and the molecular mechanisms that regulate genomic imprinting. To illustrate these concepts we review the clinical and molecular features of several human imprinting syndromes including Beckwith–Wiedemann syndrome, Silver–Russell syndrome, Angelman syndrome, Prader–Willi syndrome, pseudohypoparathyroidism, transient neonatal diabetes, familial complete hydatidiform moles and chromosome 14q32 imprinting domain disorders." @default.
- W2124234443 created "2016-06-24" @default.
- W2124234443 creator A5033933023 @default.
- W2124234443 creator A5056034710 @default.
- W2124234443 date "2009-12-01" @default.
- W2124234443 modified "2023-09-25" @default.
- W2124234443 title "Human imprinting syndromes" @default.
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