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Article

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

The New England journal of medicine - 19 Mar 1992

Smeets D F, Hamel B C, Nelen M R, Smeets H J, Bollen J H, Smits A P, Ropers H H, van Oost B A

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Share to Alleles
Share to Child, Preschool
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 15

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Paternity

Share to Prader-Willi Syndrome

Share to Translocation, Genetic

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Identifiers

PMID: 1538725
DOI: 10.1056/NEJM199203193261206

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15.PMID 1538725Read ↗

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

Paternal uniparental disomy in a child with a balanced 15;15 translocation and Angelman syndrome.Semantic proximity Read ↗

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

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

Uniparental paternal disomy in Angelman's syndrome.Semantic proximity Read ↗

Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome.Semantic proximity Read ↗

Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15).Semantic proximity Read ↗

A genetic model for the Prader-Willi syndrome and its implication for Angelman syndrome.Semantic proximity Read ↗

The Prader-Willi syndrome and the Angelman syndrome.Semantic proximity Read ↗

Microdeletion 15q26.2qter and Microduplication 18q23 in a Patient with Prader-Willi-Like Syndrome: Clinical Findings.Semantic proximity Read ↗

Comparison of the 15q deletions in Prader‐Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequencesSemantic proximity Read ↗

[Genetic basis of Prader-Willi and Angelman syndromes: implications for the biologic diagnosis].Semantic proximity Read ↗

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