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Investigation of methylation profiles in Silver-Russell syndrome to explore episignatures.
Maternal uniparental disomy of chromosome 7: how chromosome 7-encoded imprinted genes contribute to the Silver-Russell phenotype.
Rare Causes and Differential Diagnosis in Patients With Silver-Russell Syndrome.
A 79-kb paternally inherited 7q32.2 microdeletion involving MEST in a patient with a Silver-Russell syndrome-like phenotype.
Segmental maternal uniparental disomy of chromosome 7q in a patient with congenital chloride diarrhea.