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Article

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

Clinical genetics - 1 Oct 2007

Saitoh S, Hosoki K, Takano K, Tonoki H

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Share to Chromosome Aberrations
Share to Chromosome Inversion
Share to Chromosomes, Human, Pair 15
Share to DNA Methylation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Duplication

Share to Mosaicism

Share to Prader-Willi Syndrome

Share to Uniparental Disomy

Source

Identifiers

PMID: 17850637
DOI: 10.1111/j.1399-0004.2007.00860.x

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mosaic paternally derived inv dup(15) may partially rescue the Prader-Willi syndrome phenotype with uniparental disomy.PMID 17850637Read ↗

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

Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy.Semantic proximity Read ↗

Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome.Semantic proximity Read ↗

Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with mosaic trisomy 15.Semantic proximity Read ↗

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

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

Maternal age effect on the development of Prader–Willi syndrome resulting from upd(15)mat through meiosis 1 errorsSemantic proximity Read ↗

Unusual features in children with inv dup(15) supernumerary marker: a study of genotype-phenotype correlation in Taiwan.Semantic proximity Read ↗

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

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

Clinical and molecular analysis of five inv dup(15) patients.Semantic proximity Read ↗

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