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Article

Familial unbalanced translocation t(8;15)(p23.3;q11) with uniparental disomy in Angelman syndrome

1 Apr 1994

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8168819
DOI: 10.1007/bf00201679

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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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Familial unbalanced translocation t(8;15)(p23.3;q11) with uniparental disomy in Angelman syndromePMID 8168819Read ↗

Angelman Syndrome Caused by Chromosomal Rearrangements: A Case Report of 46,XX,+der(13)t(13;15)(q14.1;q12)mat,-15 with an Atypical Phenotype and Review of the Literature.Semantic proximity Read ↗

Maternal uniparental disomy 15 in a fetus resulting from a balanced familial translocation t(2;15)(p11;q11.2)Semantic proximity Read ↗

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

Girl with monosomy 1p36 and Angelman syndrome due to unbalanced der(1) transmission of a maternal translocation t(1;15)(p36.3;q13.1)Semantic proximity Read ↗

Inherited unbalanced subtelomeric translocation in a child with 8p- and Angelman syndromes.Semantic proximity Read ↗

A de novo 15q13.2q13.3 deletion in a boy with an Angelman syndrome like phenotype.Semantic proximity Read ↗

Clinical pre- and postnatal (step-by-step) history of a boy with unbalanced translocation--t(3;15)(q26.33;q26.1).Semantic proximity Read ↗

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

Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS-like phenotype.Semantic proximity Read ↗

Deletion of UBE3A in brothers with Angelman syndrome at the breakpoint with an inversion at 15q11.2.Semantic proximity Read ↗

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

Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation.Semantic proximity Read ↗

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