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

Prenatal detection of de novo inversion of chromosome 9 with duplicated heterochromatic region and postnatal follow-up.

Experimental & molecular medicine - 30 Sept 1999

Kim J J, Rhee H S, Chung Y T, Park S Y, Choi S K

Abstract excerpt

We report the first de novo case of a heterochromatic duplication on the long arm of the chromosome 9, which then was pericentrically inverted at p11q13. This condition was detected prenatally and carry to term. We then performed the follow up for over 1 year. So far, there seems to be no phenotypical abnormalities.

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Banding
Share to Chromosome Inversion
Share to Chromosomes, Human, Pair 11

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

Share to Chromosomes, Human, Pair 9

Share to Gene Duplication

Share to Karyotyping

Share to Prenatal Diagnosis

Share to Translocation, Genetic

Source

Identifiers

PMID: 10551261
DOI: 10.1038/emm.1999.22

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

Prenatal detection of de novo inversion of chromosome 9 with duplicated heterochromatic region and postnatal follow-up.PMID 10551261Read ↗

Unusual Duplication in the Pericentromeric Region of Chromosome 9 in a Patient with Phenotypic Alterations.Semantic proximity Read ↗

Maternal isodisomy of chromosome 9 with no impact on the phenotype in a woman with two isochromosomes: i(9p) and i(9q).Semantic proximity Read ↗

Duplication of 9 p11.2-p13.1: a benign cytogenetic variant.Semantic proximity Read ↗

Extreme variant of enlarged heterochromatin region on chromosome 9Q in a normal child and multiple family members.Semantic proximity Read ↗

Clinical and molecular delineation of Tetrasomy 9p syndrome: report of 12 new cases and literature review.Semantic proximity Read ↗

Correlation of clinical phenotype with a pericentric inversion of chromosome 9 and genetic counseling.Semantic proximity Read ↗

Prenatal Diagnosis of a Female Fetus with Ring Chromosome 9, 46,XX,r(9)(p24q34), and a de novo Interstitial 9p DeletionSemantic proximity Read ↗

Duplication 9p and their implication to phenotype.Semantic proximity Read ↗

[Correlation of the clinical phenotype with a pericentric inversion of chromosome 9].Semantic proximity Read ↗

Tandem duplication/deletion in a maternally derived chromosome 9 supernumerary derivative resulting in 9p trisomy and partial 9q tetrasomy.Semantic proximity Read ↗

An unusual familial chromosome 9 "variant" with variable phenotype: characterization by CGH analysis.Semantic proximity Read ↗

Heteromorphic variants of chromosome 9Semantic proximity Read ↗

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