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Article

Further patient with Angelman syndrome due to paternal disomy of chromosome 15 and a milder phenotype.

American journal of medical genetics - 10 Apr 1995

Gillessen-Kaesbach G, Albrecht B, Passarge E, Horsthemke B

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Share to Angelman Syndrome
Share to Chromosomes, Human, Pair 15
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 7778602
DOI: 10.1002/ajmg.1320560324

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

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Further patient with Angelman syndrome due to paternal disomy of chromosome 15 and a milder phenotype.PMID 7778602Read ↗

Severe phenotype in Angelman syndrome resulting from paternal isochromosome 15.Semantic proximity Read ↗

A further Angelman syndrome patient with UPD15 due to paternal meiosis II nondisjunction.Semantic proximity Read ↗

Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype?Semantic proximity Read ↗

Genotype and phenotype in Angelman syndrome caused by paternal UPD 15.Semantic proximity Read ↗

Atypical features in Angelman syndrome due to imprinting defect of uniparental disomy of chromosome 15.Semantic proximity Read ↗

Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15.Semantic proximity Read ↗

A supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotype.Semantic proximity Read ↗

Molecular and cytogenetic analyses of a patient with Prader-Willi syndrome who also had the phenotype of Angelman syndromeSemantic proximity Read ↗

A further case of a Prader-Willi syndrome phenotype in a patient with Angelman syndrome molecular defect.Semantic proximity Read ↗

Interstitial 4p deletion in a child with an Angelman syndrome-like phenotype.Semantic proximity Read ↗

Maternal origin of 15q11–13 deletions in Angelman syndrome suggests a role for genomic imprintingSemantic proximity Read ↗

[Genetic and clinical study on 17 cases of Angelman syndrome with deletion of 15q11-13].Semantic proximity Read ↗

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