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Article

UPD 13: no indication of maternal or paternal imprinting of genes on chromosome 13.

1 Jun 1995

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Share to Genetic Syndromes and Imprinting
Share to Prenatal Screening and Diagnostics

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 7666408
DOI: 10.1136/jmg.32.6.493

Provenance

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

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

UPD 13: no indication of maternal or paternal imprinting of genes on chromosome 13.PMID 7666408Read ↗

Paternal isodisomy 13 in a normal newborn infant after trisomy rescue evidenced by prenatal diagnosis.Semantic proximity Read ↗

A 10.7 Mb interstitial deletion of 13q21 without phenotypic effect defines a further non-pathogenic euchromatic variant.Semantic proximity Read ↗

Maternal uniparental disomy of chromosome 13 in a phenotypically normal child.Semantic proximity Read ↗

Search for imprinted regions on chromosome 14: Comparison of maternal and paternal UPD cases with cases of chromosome 14 deletionSemantic proximity Read ↗

Duplication 14(q24.3q31) in a father and daughter: delineation of a possible imprinted region.Semantic proximity Read ↗

Abnormal phenotypes in uniparental disomy (UPD): fundamental aspects and a critical review with bibliography of UPD other than 15.Semantic proximity Read ↗

Prenatal genetic testing for a microdeletion at chromosome 14q32.2 imprinted region leading to UPD(14)pat-like phenotype.Semantic proximity Read ↗

Maternal uniparental disomy for chromosome 14.Semantic proximity Read ↗

The IPW gene is imprinted and is not expressed in the Prader-Willi syndrome.Semantic proximity Read ↗

Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.Semantic proximity Read ↗

Uniparental isodisomy 13 in a normal female due to transmission of a maternal t(13q13q)Semantic proximity Read ↗

Trisomy 13 due to rea(13q;13q) is caused by i(13) and not rob(13;13)(q10;q10) in the majority of casesSemantic proximity Read ↗

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