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

Changes in an inherited ring (22) due to meiotic recombination? Implications for genetic counseling.

American journal of medical genetics. Part A - 1 Jun 2009

Jobanputra Vaidehi, Ash Erin, Anyane-Yeboa Kwame, Warburton Dorothy, Levy Brynn

Abstract excerpt

No abstract is available from the source.

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 Chromosomes, Human, Pair 22
Share to Developmental Disabilities
Share to Genetic Counseling

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to In Situ Hybridization, Fluorescence

Share to Karyotyping

Share to Meiosis

Share to Ring Chromosomes

Source

Identifiers

PMID: 19449399
DOI: 10.1002/ajmg.a.32680

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Changes in an inherited ring (22) due to meiotic recombination? Implications for genetic counseling.PMID 19449399Read ↗

[Progress in research and prenatal diagnosis for ring chromosomes].Semantic proximity Read ↗

Prenatal diagnosis and molecular characterization of two constitutional rings derived from one chromosome 22.Semantic proximity Read ↗

Live-born autosomal ring chromosomes at the Johns Hopkins Hospital Cytogenomics Laboratory: Case series-Spanning 52 years of experience in a single center.Semantic proximity Read ↗

[Ring chromosome 22 in a case].Semantic proximity Read ↗

Formation of a familial ring chromosome 18 investigated by SNP-array analysis.Semantic proximity Read ↗

Meiotic Recombination and Spatial Proximity in the Etiology of the Recurrent t(11;22)Semantic proximity Read ↗

Ring chromosomes: from formation to clinical potentialSemantic proximity Read ↗

Autosomal ring chromosomes in human genetic disorders.Semantic proximity Read ↗

Molecular characterization of an inherited ring (19) demonstrating ring openingSemantic proximity Read ↗

[Clinical and genetic consequences of ring chromosome, a structural genome mutation].Semantic proximity Read ↗

Inherited ring chromosomes: an analysis of published cases.Semantic proximity Read ↗

Ring chromosome 12 and severe oligospermia: a case reportSemantic proximity Read ↗

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