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Article

Deletion and uniparental disomy involving the same maternal chromosome 15.

The New England journal of medicine - 24 Feb 1994

Surh L C, Wang H, Hunter A G

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Share to Alleles
Share to Angelman Syndrome
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 15

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 8302329
DOI: 10.1056/NEJM199402243300813

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Related research

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Deletion and uniparental disomy involving the same maternal chromosome 15.PMID 8302329Read ↗

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

Uniparental disomy (UPD) other than 15: phenotypes and bibliography updated.Semantic proximity Read ↗

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

Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array‐CGHSemantic proximity Read ↗

Mosaic paternally derived inv dup(15) may partially rescue the Prader-Willi syndrome phenotype with uniparental disomy.Semantic proximity Read ↗

Parental imbalances involving chromosomes 15q and 22q may predispose to the formation of de novo pathogenic microdeletions and microduplications in the offspring.Semantic proximity Read ↗

De novo interstitial duplication of 15q11.2-q13.1 with complex maternal uniparental trisomy for the 15q11-q13 region in a patient with Prader-Willi syndrome.Semantic proximity Read ↗

Inv dup(15) supernumerary marker chromosomes.Semantic proximity Read ↗

Prader-Willi syndrome and Tay-Sachs disease in association with mixed maternal uniparental isodisomy and heterodisomy 15 in a girl who also had isochromosome Xq.Semantic proximity Read ↗

Prenatal diagnosis of a homologous Robertsonian translocation involving chromosome 15Semantic proximity Read ↗

A case which further refines the critical region for 15q25.2 microduplication phenotypes.Semantic proximity Read ↗

Severe intrauterine growth restriction and trisomy 15 confined placental mosaicism: a case report and review of literatureSemantic proximity Read ↗

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