Epigenetic signatures of Silver–Russell syndrome: Table 1

Abstract excerpt

Silver–Russell syndrome (SRS) (OMIM 180860) has been recognised as a clinical entity since the 1950s; however, a molecular genetic cause remained unknown until 1997 when maternal uniparental disomy for chromosome 7 (mUPD7) was found in approximately 10% of affected individuals. The focus then turned to the identification of causative imprinted genes on chromosome 7. Over the next 10 years many of the potential...

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