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Article

A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader–Willi syndrome

10 Dec 2008

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

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 19066619
DOI: 10.1038/ejhg.2008.232

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Related research

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A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader–Willi syndromePMID 19066619Read ↗

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A Case of Prader-Willi Syndrome With a Deletion Including MAGEL2 , NDN , and MKRN3 , but Excluding SNRPN and SNORD116.Semantic proximity Read ↗

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

Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA clusterSemantic proximity Read ↗

Prader-Willi Syndrome Is Caused by Disruption of the SNRPN GeneSemantic proximity Read ↗

Prader-Willi syndrome phenotype in X chromosome anomalies: evidence for a distinct syndrome.Semantic proximity Read ↗

Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype.Semantic proximity Read ↗

Two cases of maternal uniparental disomy 14 with a phenotype overlapping with the Prader-Willi phenotype.Semantic proximity Read ↗

The neonatal phenotype of Prader-Willi syndrome.Semantic proximity Read ↗

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