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Article

A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp

16 Nov 1999

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Share to Genetic Syndromes and Imprinting
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 10647904
DOI: 10.1007/s004399900196

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A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bpPMID 10647904Read ↗

Angelman syndrome imprinting center encodes a transcriptional promoterSemantic proximity Read ↗

Angelman syndrome caused by an identical familial 1,487-kb deletion.Semantic proximity Read ↗

Genome Organization, Function, and Imprinting in Prader-Willi and Angelman SyndromesSemantic proximity Read ↗

The imprinting box of the Prader-Willi/Angelman syndrome domain.Semantic proximity Read ↗

Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation.Semantic proximity Read ↗

Structure and function of the human chromosome 15 imprinting center.Semantic proximity Read ↗

Exceptionally mild Angelman syndrome phenotype associated with an incomplete imprinting defect.Semantic proximity Read ↗

[Etiology of Angelman syndrome--new views on the mechanism of genomic imprinting].Semantic proximity Read ↗

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

[Angelman syndrome--diagnosis and therapy of genomic imprinting disorders].Semantic proximity Read ↗

A new deletion refines the boundaries of the murine Prader-Willi syndrome imprinting center.Semantic proximity Read ↗

Deletion analysis of the imprinting center region in patients with Angelman syndrome and Prader-Willi syndrome by real-time quantitative PCR.Semantic proximity Read ↗

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