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Article

Mosaic imprinting defect in a patient with an almost typical expression of the Prader–Willi syndrome

1 Dec 2004

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Share to Epigenetics and DNA Methylation
Share to Genetic Syndromes and Imprinting
Share to Prenatal Screening and Diagnostics

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15578038
DOI: 10.1038/sj.ejhg.5201337

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Mosaic imprinting defect in a patient with an almost typical expression of the Prader–Willi syndromePMID 15578038Read ↗

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