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

Heteromorphic variants of chromosome 9

1 Apr 2013

Abstract excerpt

BACKGROUND: Heterochromatic variants of pericentromere of chromosome 9 are reported and discussed since decades concerning their detailed structure and clinical meaning. However, detailed studies are scarce. Thus, here we provide the largest ever done molecular cytogenetic research based on >300 chromosome 9 heteromorphism carriers. RESULTS: In this study, 334 carriers of heterochromatic variants of chromosome 9...

Read the complete abstract on PubMed

Topics

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

Share to Genomic variations and chromosomal abnormalities
Share to Glycogen Storage Diseases and Myoclonus
Share to Microtubule and mitosis dynamics

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

Source

Identifiers

PMID: 23547710
DOI: 10.1186/1755-8166-6-14

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 17 Oct 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

Heteromorphic variants of chromosome 9PMID 23547710Read ↗

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

Variants of chromosome 9 in phenotypically normal individuals.Semantic proximity Read ↗

Polymorphic Rearrangements of Human Chromosome 9 and Male Infertility: New Evidence and Impact on SpermatogenesisSemantic proximity Read ↗

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

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

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

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

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

DNA sequence and analysis of human chromosome 9.Semantic proximity Read ↗

Pericentric inversion 9--incidence and clinical significance.Semantic proximity Read ↗

TEM, FISH and molecular studies in infertile men with pericentric inversion of chromosome 9Semantic proximity Read ↗

Polymorphic variants on chromosomes probably play a significant role in infertility.Semantic proximity Read ↗

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