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Article

Do patients with maternal uniparental disomy for chromosome 7 have a distinct mild Silver-Russell phenotype?

Journal of medical genetics - 1 Apr 2001

Hannula K, Kere J, Pirinen S, Holmberg C, Lipsanen-Nyman M

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Share to Chromosome Aberrations
Share to Chromosomes, Human, Pair 7
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 11370636
DOI: 10.1136/jmg.38.4.273
PMCID: PMC1734847

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Related research

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Do patients with maternal uniparental disomy for chromosome 7 have a distinct mild Silver-Russell phenotype?PMID 11370636Read ↗

New Developments in Silver–Russell Syndrome and Implications for Clinical PracticeSemantic proximity Read ↗

Maternal uniparental disomy 7 in Silver-Russell syndrome.Semantic proximity Read ↗

A Narrow Segment of Maternal Uniparental Disomy of Chromosome 7q31-qter in Silver-Russell Syndrome Delimits a Candidate Gene RegionSemantic proximity Read ↗

Clinical and molecular findings in two patients with russell-silver syndrome and UPD7: comparison with non-UPD7 cases.Semantic proximity Read ↗

The genetic aetiology of Silver-Russell syndrome.Semantic proximity Read ↗

Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region.Semantic proximity Read ↗

Genetics of Silver-Russell syndrome.Semantic proximity Read ↗

An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands.Semantic proximity Read ↗

[Uniparental disomy 7 in the pathogenesis of Silver-Russell syndrome].Semantic proximity Read ↗

Russell-Silver syndrome: molecular diagnosis of maternal uniparental disomy of chromosome 7 using methylation-specific polymerase chain reaction assay and single nucleotide polymorphisms genotyping.Semantic proximity Read ↗

Epigenetic and genetic diagnosis of Silver-Russell syndrome.Semantic proximity Read ↗

Epigenetic signatures of Silver–Russell syndrome: Table 1Semantic proximity Read ↗

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