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

Significance of a prenatally diagnosed del(10)(q23)

28 Nov 2001

Abstract excerpt

Structural chromosome mosaicism is rare. We report a case of prenatal mosaicism for a deletion of chromosome 10(q23). To our knowledge, there are only three reports of prenatally diagnosed cases of del(10)(q23). Two of these cases were due to an inherited fragile site. In the present case amniocentesis revealed 46,XY,del(10)(q23)[9]/46,XY[45]. Follow-up chromosome analysis of peripheral blood and placental tissue...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomal and Genetic Variations
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 11807894
DOI: 10.1002/ajmg.10112

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 · 9 closest

Significance of a prenatally diagnosed del(10)(q23)PMID 11807894Read ↗

Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicism.Semantic proximity Read ↗

Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype.Semantic proximity Read ↗

Trisomy 10 mosaicism and maternal uniparental disomy 10 in a liveborn infant with severe congenital malformations.Semantic proximity Read ↗

Familial deletion of (8)(q24.13q24.22) associated with a normal phenotype.Semantic proximity Read ↗

Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH).Semantic proximity Read ↗

Prenatal diagnosis of trisomy 9 mosaicism possibly limited to fetal membranes.Semantic proximity Read ↗

Inv(10)(p11.2q21.2), a variant chromosome.Semantic proximity Read ↗

“Pseudomosaicism” for 4p – in amniotic fluid cell culture proven to be true mosaicism after birthSemantic proximity Read ↗

A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).Semantic proximity Read ↗

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