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Article

Maternal Uniparental Disomy of Chromosome 1 with No Apparent Phenotypic Effects

1 Oct 1998

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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 Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 9758608
DOI: 10.1086/302050

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Click a neighbor to travelStep 1 · 12 closest

Maternal Uniparental Disomy of Chromosome 1 with No Apparent Phenotypic EffectsPMID 9758608Read ↗

Uniparental disomy with normal phenotype.Semantic proximity Read ↗

Supernumerary marker chromosome (1) of paternal origin and maternal uniparental disomy 1 in a developmentally delayed child.Semantic proximity Read ↗

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

A transmitted deletion of 2q13 to 2q14.1 causes no phenotypic abnormalities.Semantic proximity Read ↗

Maternal uniparental disomy of chromosome 13 in a phenotypically normal child.Semantic proximity Read ↗

Normal phenotype with maternal isodisomy in a female with two isochromosomes: i(2p) and i(2q)Semantic proximity Read ↗

Maternal uniparental isodisomy 11q13qter in a dysmorphic and mentally retarded female with partial trisomy mosaicism 11q13qter.Semantic proximity Read ↗

Maternal uniparental disomy 22 has no impact on the phenotype.Semantic proximity Read ↗

Paternal uniparental disomy for chromosome 1 revealed by molecular analysis of a patient with pycnodysostosis.Semantic proximity Read ↗

Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18Semantic proximity Read ↗

An unexpected transmission of von Willebrand disease type 3: the first case of maternal uniparental disomy 12.Semantic proximity Read ↗

Maternal uniparental disomy for chromosome 14.Semantic proximity Read ↗

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