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Article

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

1 Jan 2001

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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: 11112662
DOI: 10.1086/316937

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Related research

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A Narrow Segment of Maternal Uniparental Disomy of Chromosome 7q31-qter in Silver-Russell Syndrome Delimits a Candidate Gene RegionPMID 11112662Read ↗

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

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

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

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

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

Clinical utility gene card for: Williams-Beuren Syndrome [7q11.23].Semantic proximity Read ↗

Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell SyndromeSemantic proximity Read ↗

Silver-Russell Syndrome - Part I: Clinical Characteristics and Genetic Background.Semantic proximity Read ↗

Maternally inherited duplication of chromosome 7, dup(7)(p11.2p12), associated with mild cognitive deficit without features of Silver–Russell syndromeSemantic proximity Read ↗

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneitySemantic proximity Read ↗

Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions.Semantic proximity Read ↗

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