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Oxford University Press

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Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci

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Human Molecular Genetics, Vol. 18, Iss. 24, 2009-12 ,pp. : 4724-4733

Oxford University Press

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Microduplication of the ICR2 domain at chromosome 11p15 and familial Silver–Russell syndrome

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John Wiley & Sons Inc

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Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith–Wiedemann syndrome and Silver–Russell syndrome

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Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular Etiology

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