Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Comparative analysis of isodisomic and heterodisomic segments in cases with maternal uniparental disomy 14 suggests more than one imprinted region.

Clinical genetics - 1 Sept 2001

Kotzot D

Abstract excerpt

The results of molecular investigations of 21 cases with complete or segmental maternal uniparental disomy (UPD) 14 published in the literature were compared with respect to isodisomic and heterodisomic segments. The aim of the study was to find hints toward imprinted regions other than the recently defined imprinted segment 14q32. Three regions with no isodisomic molecular marker were found. The most distal of...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosome Mapping
Share to Chromosomes, Human, Pair 14
Share to Databases as Topic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genomic Imprinting

Share to MEDLINE

Share to Mothers

Share to Software

Share to Uniparental Disomy

Source

Identifiers

PMID: 11595025
DOI: 10.1034/j.1399-0004.2001.600309.x

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Comparative analysis of isodisomic and heterodisomic segments in cases with maternal uniparental disomy 14 suggests more than one imprinted region.PMID 11595025Read ↗

Maternally inherited duplication of the possible imprinted 14q31 region.Semantic proximity Read ↗

Maternal isodisomy for 14q21-q24 in a man with diabetes mellitus.Semantic proximity Read ↗

A case of segmental paternal isodisomy of chromosome 14.Semantic proximity Read ↗

Segmental and full paternal isodisomy for chromosome 14 in three patients: Narrowing the critical region and implication for the clinical featuresSemantic proximity Read ↗

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

Complex and segmental uniparental disomy updatedSemantic proximity Read ↗

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

Epimutation at human chromosome 14q32.2 in a boy with a upd(14)mat-like clinical phenotype.Semantic proximity Read ↗

Cytogenetic contribution to uniparental disomy (UPD)Semantic proximity Read ↗

Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes.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 ↗

Paternal uniparental isodisomy for chromosome 14 in a patient with a normal 46,XY karyotype.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.